Canonical Allele Identifier: CA2832959
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs553904309
ExAC: 4:4862016 G / A
gnomAD v2: 4-4862016-G-A
gnomAD v4: 4-4860289-G-A
MyVariant Identifiers: chr4:g.4862016G>A (hg19) chr4:g.4860289G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860289G>A , CM000666.2:g.4860289G>A GRCh38
NC_000004.11:g.4862016G>A , CM000666.1:g.4862016G>A GRCh37
NC_000004.10:g.4912917G>A NCBI36
NG_008121.1:g.5625G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.390G>A MANE Select ENSP00000372170.4:p.Ala130=
ENST00000382723.4:c.390G>A ENSP00000372170.4:p.Ala130=
NM_002448.3:c.390G>A MANE Select NP_002439.2:p.Ala130=
Search 100 bp 5'
Search 100 bp 3'