Canonical Allele Identifier: CA947696904
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1940333145

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447695G>A , CM000674.2:g.52447695G>A GRCh38
NC_000012.11:g.52841479G>A , CM000674.1:g.52841479G>A GRCh37
NC_000012.10:g.51127746G>A NCBI36
NG_008299.1:g.9432C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1424+83C>T MANE Select ENSP00000252252.3:n.1424+83C>T
ENST00000252252.3:c.1424+83C>T ENSP00000252252.3:n.1424+83C>T
NM_005555.3:c.1424+83C>T NP_005546.2:n.1424+83C>T
NM_005555.4:c.1424+83C>T MANE Select NP_005546.2:n.1424+83C>T