Canonical Allele Identifier: CA2036500225
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1940399049

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451330T>G , CM000674.2:g.52451330T>G GRCh38
NC_000012.11:g.52845114T>G , CM000674.1:g.52845114T>G GRCh37
NC_000012.10:g.51131381T>G NCBI36
NG_008299.1:g.5797A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+209A>C MANE Select ENSP00000252252.3:n.540+209A>C
ENST00000252252.3:c.540+209A>C ENSP00000252252.3:n.540+209A>C
NM_005555.3:c.540+209A>C NP_005546.2:n.540+209A>C
NM_005555.4:c.540+209A>C MANE Select NP_005546.2:n.540+209A>C