Canonical Allele Identifier: CA2624233660
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

gnomAD v4: 14-23415843-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415843G>T , CM000676.2:g.23415843G>T GRCh38
NC_000014.8:g.23885052G>T , CM000676.1:g.23885052G>T GRCh37
NC_000014.7:g.22954892G>T NCBI36
NG_007884.1:g.24819C>A , LRG_384:g.24819C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4954-11C>A (MYH7) MANE Select ENSP00000347507.3:n.4954-11C>A
ENST00000355349.3:c.4954-11C>A (MYH7) ENSP00000347507.3:n.4954-11C>A
NM_000257.3:c.4954-11C>A (MYH7) NP_000248.2:n.4954-11C>A
NR_126491.1:n.261+14G>T (MHRT)
XM_017021340.1:c.4954-11C>A (MYH7) XP_016876829.1:n.4954-11C>A
NM_000257.4:c.4954-11C>A (MYH7) MANE Select NP_000248.2:n.4954-11C>A
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