Canonical Allele Identifier: CA384927183

Gene: KRT6B

Linked Data

• MyVariant Identifiers: chr12:g.52845382C>G (hg19) ; chr12:g.52451598C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451598C>G , CM000674.2:g.52451598C>G	GRCh38
NC_000012.11:g.52845382C>G , CM000674.1:g.52845382C>G	GRCh37
NC_000012.10:g.51131649C>G	NCBI36
NG_008299.1:g.5529G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.481G>C MANE Select	ENSP00000252252.3:p.Ala161Pro
ENST00000252252.3:c.481G>C	ENSP00000252252.3:p.Ala161Pro
NM_005555.3:c.481G>C	NP_005546.2:p.Ala161Pro
NM_005555.4:c.481G>C MANE Select	NP_005546.2:p.Ala161Pro