Canonical Allele Identifier: CA041893

Linked Data

ClinVar Variation Id: 698942
ClinVar RCV Id: RCV000866576
dbSNP Id: rs201253277

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417495G>T , CM000676.2:g.23417495G>T GRCh38
NC_000014.8:g.23886704G>T , CM000676.1:g.23886704G>T GRCh37
NC_000014.7:g.22956544G>T NCBI36
NG_007884.1:g.23167C>A , LRG_384:g.23167C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+8C>A (MYH7) MANE Select ENSP00000347507.3:n.4353+8C>A
ENST00000355349.3:c.4353+8C>A (MYH7) ENSP00000347507.3:n.4353+8C>A
NM_000257.3:c.4353+8C>A (MYH7) NP_000248.2:n.4353+8C>A
NR_126491.1:n.814-38G>T (MHRT)
XM_017021340.1:c.4353+8C>A (MYH7) XP_016876829.1:n.4353+8C>A
NM_000257.4:c.4353+8C>A (MYH7) MANE Select NP_000248.2:n.4353+8C>A