Canonical Allele Identifier: CA356137613
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4860189-G-C
MyVariant Identifiers: chr4:g.4861916G>C (hg19) chr4:g.4860189G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860189G>C , CM000666.2:g.4860189G>C GRCh38
NC_000004.11:g.4861916G>C , CM000666.1:g.4861916G>C GRCh37
NC_000004.10:g.4912817G>C NCBI36
NG_008121.1:g.5525G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.290G>C MANE Select ENSP00000372170.4:p.Gly97Ala
ENST00000382723.4:c.290G>C ENSP00000372170.4:p.Gly97Ala
NM_002448.3:c.290G>C MANE Select NP_002439.2:p.Gly97Ala
Search 100 bp 5'
Search 100 bp 3'