Canonical Allele Identifier: CA398122659
Gene: MYH8 HGNC NCBI
MYHAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.10312476T>G (hg19) chr17:g.10409159T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10409159T>G , CM000679.2:g.10409159T>G GRCh38
NC_000017.10:g.10312476T>G , CM000679.1:g.10312476T>G GRCh37
NC_000017.9:g.10253201T>G NCBI36
NG_013015.1:g.17792A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403437.2:c.1903A>C (MYH8) MANE Select ENSP00000384330.2:p.Ser635Arg
NM_002472.2:c.1903A>C (MYH8) NP_002463.2:p.Ser635Arg
NR_125367.1:n.167+2921T>G (MYHAS)
XM_011523873.1:c.1903A>C (MYH8) XP_011522175.1:p.Ser635Arg
XM_011523874.1:c.1903A>C (MYH8) XP_011522176.1:p.Ser635Arg
NM_002472.3:c.1903A>C (MYH8) MANE Select NP_002463.2:p.Ser635Arg
Search 100 bp 5'
Search 100 bp 3'