Canonical Allele Identifier: CA8387971

Linked Data

ClinVar Variation Id: 750566
dbSNP Id: rs151091483

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10409361A>T , CM000679.2:g.10409361A>T GRCh38
NC_000017.10:g.10312678A>T , CM000679.1:g.10312678A>T GRCh37
NC_000017.9:g.10253403A>T NCBI36
NG_013015.1:g.17590T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403437.2:c.1815T>A (MYH8) MANE Select ENSP00000384330.2:p.Asn605Lys
NM_002472.2:c.1815T>A (MYH8) NP_002463.2:p.Asn605Lys
NR_125367.1:n.167+3123A>T (MYHAS)
XM_011523873.1:c.1815T>A (MYH8) XP_011522175.1:p.Asn605Lys
XM_011523874.1:c.1815T>A (MYH8) XP_011522176.1:p.Asn605Lys
NM_002472.3:c.1815T>A (MYH8) MANE Select NP_002463.2:p.Asn605Lys