Canonical Allele Identifier: CA384926147

Gene: KRT6B

Linked Data

• MyVariant Identifiers: chr12:g.52845321A>T (hg19) ; chr12:g.52451537A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451537A>T , CM000674.2:g.52451537A>T	GRCh38
NC_000012.11:g.52845321A>T , CM000674.1:g.52845321A>T	GRCh37
NC_000012.10:g.51131588A>T	NCBI36
NG_008299.1:g.5590T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.540+2T>A MANE Select	ENSP00000252252.3:n.540+2T>A
ENST00000252252.3:c.540+2T>A	ENSP00000252252.3:n.540+2T>A
NM_005555.3:c.540+2T>A	NP_005546.2:n.540+2T>A
NM_005555.4:c.540+2T>A MANE Select	NP_005546.2:n.540+2T>A