Canonical Allele Identifier: CA356138954

Gene: MSX1

Linked Data

• dbSNP Id: rs1577536879
• gnomAD v3: 4-4863049-G-C
• gnomAD v4: 4-4863049-G-C
• MyVariant Identifiers: chr4:g.4864776G>C (hg19) ; chr4:g.4863049G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4863049G>C , CM000666.2:g.4863049G>C	GRCh38
NC_000004.11:g.4864776G>C , CM000666.1:g.4864776G>C	GRCh37
NC_000004.10:g.4915677G>C	NCBI36
NG_008121.1:g.8385G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.818G>C MANE Select	ENSP00000372170.4:p.Gly273Ala
ENST00000382723.4:c.818G>C	ENSP00000372170.4:p.Gly273Ala
NM_002448.3:c.818G>C MANE Select	NP_002439.2:p.Gly273Ala