Canonical Allele Identifier: CA1435013583
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1472789620

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862672C>G , CM000666.2:g.4862672C>G GRCh38
NC_000004.11:g.4864399C>G , CM000666.1:g.4864399C>G GRCh37
NC_000004.10:g.4915300C>G NCBI36
NG_008121.1:g.8008C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-29C>G MANE Select ENSP00000372170.4:n.470-29C>G
ENST00000382723.4:c.470-29C>G ENSP00000372170.4:n.470-29C>G
ENST00000468421.1:n.182-29C>G
NM_002448.3:c.470-29C>G MANE Select NP_002439.2:n.470-29C>G