Canonical Allele Identifier: CA8548967
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs367803772

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867096T>C , CM000679.2:g.40867096T>C GRCh38
NC_000017.10:g.39023348T>C , CM000679.1:g.39023348T>C GRCh37
NC_000017.9:g.36276874T>C NCBI36
NG_008077.1:g.5115A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.91A>G MANE Select ENSP00000251643.4:p.Arg31Gly
ENST00000647902.1:c.91A>G ENSP00000497770.1:p.Arg31Gly
ENST00000251643.4:c.91A>G ENSP00000251643.4:p.Arg31Gly
NM_000223.3:c.91A>G NP_000214.1:p.Arg31Gly
XR_934754.1:n.1500+16236T>C
XR_934754.2:n.2008+16236T>C
NM_000223.4:c.91A>G MANE Select NP_000214.1:p.Arg31Gly