Canonical Allele Identifier: CA704289126
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1483339420
gnomAD v3: 14-23420676-C-A
gnomAD v4: 14-23420676-C-A
MyVariant Identifiers: chr14:g.23889885C>A (hg19) chr14:g.23420676C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420676C>A , CM000676.2:g.23420676C>A GRCh38
NC_000014.8:g.23889885C>A , CM000676.1:g.23889885C>A GRCh37
NC_000014.7:g.22959725C>A NCBI36
NG_007884.1:g.19986G>T , LRG_384:g.19986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+282G>T MANE Select ENSP00000347507.3:n.3336+282G>T
ENST00000355349.3:c.3336+282G>T ENSP00000347507.3:n.3336+282G>T
NM_000257.3:c.3336+282G>T NP_000248.2:n.3336+282G>T
XR_245686.3:n.3444+282G>T
XM_017021340.1:c.3336+282G>T XP_016876829.1:n.3336+282G>T
NM_000257.4:c.3336+282G>T MANE Select NP_000248.2:n.3336+282G>T
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