Canonical Allele Identifier: CA384927237
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451621T>A , CM000674.2:g.52451621T>A GRCh38
NC_000012.11:g.52845405T>A , CM000674.1:g.52845405T>A GRCh37
NC_000012.10:g.51131672T>A NCBI36
NG_008299.1:g.5506A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.458A>T MANE Select ENSP00000252252.3:p.Asp153Val
ENST00000252252.3:c.458A>T ENSP00000252252.3:p.Asp153Val
NM_005555.3:c.458A>T NP_005546.2:p.Asp153Val
NM_005555.4:c.458A>T MANE Select NP_005546.2:p.Asp153Val