Canonical Allele Identifier: CA6580827
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs757382249
COSMIC: COSM940727

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451596G>A , CM000674.2:g.52451596G>A GRCh38
NC_000012.11:g.52845380G>A , CM000674.1:g.52845380G>A GRCh37
NC_000012.10:g.51131647G>A NCBI36
NG_008299.1:g.5531C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.483C>T MANE Select ENSP00000252252.3:p.Ala161=
ENST00000252252.3:c.483C>T ENSP00000252252.3:p.Ala161=
NM_005555.3:c.483C>T NP_005546.2:p.Ala161=
NM_005555.4:c.483C>T MANE Select NP_005546.2:p.Ala161=