Canonical Allele Identifier: CA704271375
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1352588714
MyVariant Identifiers: chr14:g.23903245C>T (hg19) chr14:g.23434036C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23434036C>T , CM000676.2:g.23434036C>T GRCh38
NC_000014.8:g.23903245C>T , CM000676.1:g.23903245C>T GRCh37
NC_000014.7:g.22973085C>T NCBI36
NG_007884.1:g.6626G>A , LRG_384:g.6626G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-9+158G>A MANE Select ENSP00000347507.3:n.-9+158G>A
ENST00000355349.3:c.-9+158G>A ENSP00000347507.3:n.-9+158G>A
NM_000257.3:c.-9+158G>A NP_000248.2:n.-9+158G>A
XR_245686.3:n.98+158G>A
XM_017021340.1:c.-8-296G>A XP_016876829.1:n.-8-296G>A
NM_000257.4:c.-9+158G>A MANE Select NP_000248.2:n.-9+158G>A
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