Canonical Allele Identifier: CA384927475
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451669T>C , CM000674.2:g.52451669T>C GRCh38
NC_000012.11:g.52845453T>C , CM000674.1:g.52845453T>C GRCh37
NC_000012.10:g.51131720T>C NCBI36
NG_008299.1:g.5458A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.410A>G MANE Select ENSP00000252252.3:p.Glu137Gly
ENST00000252252.3:c.410A>G ENSP00000252252.3:p.Glu137Gly
NM_005555.3:c.410A>G NP_005546.2:p.Glu137Gly
NM_005555.4:c.410A>G MANE Select NP_005546.2:p.Glu137Gly