Canonical Allele Identifier: CA689838565

Gene: KRT6B

Linked Data

• dbSNP Id: rs1297262634
• gnomAD v3: 12-52451523-C-A
• gnomAD v4: 12-52451523-C-A
• MyVariant Identifiers: chr12:g.52845307C>A (hg19) ; chr12:g.52451523C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52451523C>A , CM000674.2:g.52451523C>A	GRCh38
NC_000012.11:g.52845307C>A , CM000674.1:g.52845307C>A	GRCh37
NC_000012.10:g.51131574C>A	NCBI36
NG_008299.1:g.5604G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252252.4:c.540+16G>T MANE Select	ENSP00000252252.3:n.540+16G>T
ENST00000252252.3:c.540+16G>T	ENSP00000252252.3:n.540+16G>T
NM_005555.3:c.540+16G>T	NP_005546.2:n.540+16G>T
NM_005555.4:c.540+16G>T MANE Select	NP_005546.2:n.540+16G>T