Canonical Allele Identifier: CA389052724
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 525040
ClinVar RCV Id: RCV000629022
dbSNP Id: rs1555338762
MyVariant Identifiers: chr14:g.23901866A>C (hg19) chr14:g.23432657A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23432657A>C , CM000676.2:g.23432657A>C GRCh38
NC_000014.8:g.23901866A>C , CM000676.1:g.23901866A>C GRCh37
NC_000014.7:g.22971706A>C NCBI36
NG_007884.1:g.8005T>G , LRG_384:g.8005T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.484T>G MANE Select ENSP00000347507.3:p.Tyr162Asp
ENST00000355349.3:c.484T>G ENSP00000347507.3:p.Tyr162Asp
NM_000257.3:c.484T>G NP_000248.2:p.Tyr162Asp
XR_245686.3:n.590T>G
XM_017021340.1:c.484T>G XP_016876829.1:p.Tyr162Asp
NM_000257.4:c.484T>G MANE Select NP_000248.2:p.Tyr162Asp
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Search 100 bp 3'