Canonical Allele Identifier: CA216518
Gene: KRT12 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 66128
ClinVar RCV Id: RCV000056428
dbSNP Id: rs11650915

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867144G>A , CM000679.2:g.40867144G>A GRCh38
NC_000017.9:g.36276922G>A NCBI36
NC_000017.10:g.39023396G>A , CM000679.1:g.39023396G>A GRCh37
NG_008077.1:g.5067C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251643.4:c.43C>T ENSP00000251643.4:p.Pro15Ser
NM_000223.3:c.43C>T VV NP_000214.1:p.Pro15Ser
XR_934754.1:n.1500+16284G>A