Canonical Allele Identifier: CA6580409

Gene: KRT6B

Linked Data

• dbSNP Id: rs763435088
• ExAC: 12:52841546 C / T
• gnomAD v4: 12-52447762-C-T
• MyVariant Identifiers: chr12:g.52841546C>T (hg19) ; chr12:g.52447762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52447762C>T , CM000674.2:g.52447762C>T	GRCh38
NC_000012.11:g.52841546C>T , CM000674.1:g.52841546C>T	GRCh37
NC_000012.10:g.51127813C>T	NCBI36
NG_008299.1:g.9365G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252252.4:c.1424+16G>A MANE Select	ENSP00000252252.3:n.1424+16G>A
ENST00000252252.3:c.1424+16G>A	ENSP00000252252.3:n.1424+16G>A
NM_005555.3:c.1424+16G>A	NP_005546.2:n.1424+16G>A
NM_005555.4:c.1424+16G>A MANE Select	NP_005546.2:n.1424+16G>A