Canonical Allele Identifier: CA312769
Gene: MUT HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 203850
dbSNP Id: rs753564352

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444652C>T , CM000668.2:g.49444652C>T GRCh38
NC_000006.10:g.49520324C>T NCBI36
NC_000006.11:g.49412365C>T , CM000668.1:g.49412365C>T GRCh37
NG_007100.1:g.23488G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.3:c.1663G>A ENSP00000274813.3:p.Ala555Thr
NM_000255.3:c.1663G>A NP_000246.2:p.Ala555Thr
XM_005249143.2:c.1663G>A XP_005249200.1:p.Ala555Thr