Canonical Allele Identifier: CA398155591
Gene: MYH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639362G>C , CM000679.2:g.10639362G>C GRCh38
NC_000017.10:g.10542679G>C , CM000679.1:g.10542679G>C GRCh37
NC_000017.9:g.10483404G>C NCBI36
NG_011537.1:g.22937C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.3038C>G MANE Select ENSP00000464317.1:p.Ala1013Gly
ENST00000583535.5:c.3038C>G ENSP00000464317.1:p.Ala1013Gly
NM_002470.3:c.3038C>G NP_002461.2:p.Ala1013Gly
XM_011523870.1:c.3038C>G XP_011522172.1:p.Ala1013Gly
XM_011523871.1:c.3038C>G XP_011522173.1:p.Ala1013Gly
XM_011523872.1:c.3038C>G XP_011522174.1:p.Ala1013Gly
XM_011523870.3:c.3038C>G XP_011522172.1:p.Ala1013Gly
XM_011523871.2:c.3038C>G XP_011522173.1:p.Ala1013Gly
NM_002470.4:c.3038C>G MANE Select NP_002461.2:p.Ala1013Gly