Canonical Allele Identifier: CA356138037

Gene: MSX1

Linked Data

• dbSNP Id: rs1220626727
• gnomAD v2: 4-4862032-A-G
• gnomAD v4: 4-4860305-A-G
• MyVariant Identifiers: chr4:g.4862032A>G (hg19) ; chr4:g.4860305A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4860305A>G , CM000666.2:g.4860305A>G	GRCh38
NC_000004.11:g.4862032A>G , CM000666.1:g.4862032A>G	GRCh37
NC_000004.10:g.4912933A>G	NCBI36
NG_008121.1:g.5641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.406A>G MANE Select	ENSP00000372170.4:p.Ser136Gly
ENST00000382723.4:c.406A>G	ENSP00000372170.4:p.Ser136Gly
NM_002448.3:c.406A>G MANE Select	NP_002439.2:p.Ser136Gly