Canonical Allele Identifier: CA384927202
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451603A>G , CM000674.2:g.52451603A>G GRCh38
NC_000012.11:g.52845387A>G , CM000674.1:g.52845387A>G GRCh37
NC_000012.10:g.51131654A>G NCBI36
NG_008299.1:g.5524T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.476T>C MANE Select ENSP00000252252.3:p.Val159Ala
ENST00000252252.3:c.476T>C ENSP00000252252.3:p.Val159Ala
NM_005555.3:c.476T>C NP_005546.2:p.Val159Ala
NM_005555.4:c.476T>C MANE Select NP_005546.2:p.Val159Ala