Canonical Allele Identifier: CA485767228
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23900640T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431431T>G , CM000676.2:g.23431431T>G GRCh38
NC_000014.8:g.23900640T>G , CM000676.1:g.23900640T>G GRCh37
NC_000014.7:g.22970480T>G NCBI36
NG_007884.1:g.9231A>C , LRG_384:g.9231A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.783A>C MANE Select ENSP00000347507.3:p.Ala261=
ENST00000355349.3:c.783A>C ENSP00000347507.3:p.Ala261=
NM_000257.3:c.783A>C NP_000248.2:p.Ala261=
XR_245686.3:n.889A>C
XM_017021340.1:c.783A>C XP_016876829.1:p.Ala261=
NM_000257.4:c.783A>C MANE Select NP_000248.2:p.Ala261=
Search 100 bp 5'
Search 100 bp 3'