Canonical Allele Identifier: CA119163
Gene: KRT12 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7927
dbSNP Id: rs28936695

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866801A>G , CM000679.2:g.40866801A>G GRCh38
NC_000017.10:g.39023053A>G , CM000679.1:g.39023053A>G GRCh37
NC_000017.9:g.36276579A>G NCBI36
NG_008077.1:g.5410T>C

Transcript Alleles

HGVS Amino-acid change
NM_000223.3:c.386T>C VV NP_000214.1:p.Met129Thr
XR_934754.1:n.1500+15941A>G
XR_934754.2:n.2008+15941A>G
ENST00000251643.4:c.386T>C ENSP00000251643.4:p.Met129Thr