Canonical Allele Identifier: CA1435013542
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737942782

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862620C>T , CM000666.2:g.4862620C>T GRCh38
NC_000004.11:g.4864347C>T , CM000666.1:g.4864347C>T GRCh37
NC_000004.10:g.4915248C>T NCBI36
NG_008121.1:g.7956C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-81C>T MANE Select ENSP00000372170.4:n.470-81C>T
ENST00000382723.4:c.470-81C>T ENSP00000372170.4:n.470-81C>T
ENST00000468421.1:n.181+12C>T
NM_002448.3:c.470-81C>T MANE Select NP_002439.2:n.470-81C>T