Canonical Allele Identifier: CA014878
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 179243
ClinVar RCV Id: RCV000156030
dbSNP Id: rs727504734
MyVariant Identifiers: chr14:g.23886529T>G (hg19) chr14:g.23417320T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417320T>G , CM000676.2:g.23417320T>G GRCh38
NC_000014.8:g.23886529T>G , CM000676.1:g.23886529T>G GRCh37
NC_000014.7:g.22956369T>G NCBI36
NG_007884.1:g.23342A>C , LRG_384:g.23342A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4354-2A>C (MYH7) MANE Select ENSP00000347507.3:n.4354-2A>C
ENST00000355349.3:c.4354-2A>C (MYH7) ENSP00000347507.3:n.4354-2A>C
NM_000257.3:c.4354-2A>C (MYH7) NP_000248.2:n.4354-2A>C
NR_126491.1:n.760T>G (MHRT)
XM_017021340.1:c.4354-2A>C (MYH7) XP_016876829.1:n.4354-2A>C
NM_000257.4:c.4354-2A>C (MYH7) MANE Select NP_000248.2:n.4354-2A>C
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