Canonical Allele Identifier: CA480069828
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1370643603

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492682G>C , CM000674.2:g.52492682G>C GRCh38
NC_000012.11:g.52886466G>C , CM000674.1:g.52886466G>C GRCh37
NC_000012.10:g.51172733G>C NCBI36
NG_008298.1:g.5716C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.507C>G MANE Select ENSP00000369317.3:p.Thr169=
ENST00000330722.6:c.507C>G ENSP00000369317.3:p.Thr169=
ENST00000549898.5:n.28C>G
NM_005554.3:c.507C>G NP_005545.1:p.Thr169=
NM_005554.4:c.507C>G MANE Select NP_005545.1:p.Thr169=