Canonical Allele Identifier: CA549707226
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1165120145
gnomAD v2: 4-4864366-G-A
gnomAD v3: 4-4862639-G-A
gnomAD v4: 4-4862639-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862639G>A , CM000666.2:g.4862639G>A GRCh38
NC_000004.11:g.4864366G>A , CM000666.1:g.4864366G>A GRCh37
NC_000004.10:g.4915267G>A NCBI36
NG_008121.1:g.7975G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-62G>A MANE Select ENSP00000372170.4:n.470-62G>A
ENST00000382723.4:c.470-62G>A ENSP00000372170.4:n.470-62G>A
ENST00000468421.1:n.181+31G>A
NM_002448.3:c.470-62G>A MANE Select NP_002439.2:n.470-62G>A