Canonical Allele Identifier: CA2833081
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs551697430
gnomAD v2: 4-4864562-C-G
gnomAD v3: 4-4862835-C-G
gnomAD v4: 4-4862835-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862835C>G , CM000666.2:g.4862835C>G GRCh38
NC_000004.11:g.4864562C>G , CM000666.1:g.4864562C>G GRCh37
NC_000004.10:g.4915463C>G NCBI36
NG_008121.1:g.8171C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.604C>G MANE Select ENSP00000372170.4:p.Arg202Gly
ENST00000382723.4:c.604C>G ENSP00000372170.4:p.Arg202Gly
ENST00000468421.1:n.316C>G
NM_002448.3:c.604C>G MANE Select NP_002439.2:p.Arg202Gly