Canonical Allele Identifier: CA613318025
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1337316085
gnomAD v2: 14-23887391-G-A
gnomAD v4: 14-23418182-G-A
MyVariant Identifiers: chr14:g.23887391G>A (hg19) chr14:g.23418182G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23418182G>A , CM000676.2:g.23418182G>A GRCh38
NC_000014.8:g.23887391G>A , CM000676.1:g.23887391G>A GRCh37
NC_000014.7:g.22957231G>A NCBI36
NG_007884.1:g.22480C>T , LRG_384:g.22480C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.4169+28C>T MANE Select ENSP00000347507.3:n.4169+28C>T
ENST00000355349.3:c.4169+28C>T ENSP00000347507.3:n.4169+28C>T
NM_000257.3:c.4169+28C>T NP_000248.2:n.4169+28C>T
XM_017021340.1:c.4169+28C>T XP_016876829.1:n.4169+28C>T
NM_000257.4:c.4169+28C>T MANE Select NP_000248.2:n.4169+28C>T
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