Canonical Allele Identifier: CA384927486

Gene: KRT6B

Linked Data

• MyVariant Identifiers: chr12:g.52845455T>G (hg19) ; chr12:g.52451671T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451671T>G , CM000674.2:g.52451671T>G	GRCh38
NC_000012.11:g.52845455T>G , CM000674.1:g.52845455T>G	GRCh37
NC_000012.10:g.51131722T>G	NCBI36
NG_008299.1:g.5456A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.408A>C MANE Select	ENSP00000252252.3:p.Gln136His
ENST00000252252.3:c.408A>C	ENSP00000252252.3:p.Gln136His
NM_005555.3:c.408A>C	NP_005546.2:p.Gln136His
NM_005555.4:c.408A>C MANE Select	NP_005546.2:p.Gln136His