Canonical Allele Identifier: CA384926249
Gene: KRT6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451560C>A , CM000674.2:g.52451560C>A GRCh38
NC_000012.11:g.52845344C>A , CM000674.1:g.52845344C>A GRCh37
NC_000012.10:g.51131611C>A NCBI36
NG_008299.1:g.5567G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.519G>T MANE Select ENSP00000252252.3:p.Lys173Asn
ENST00000252252.3:c.519G>T ENSP00000252252.3:p.Lys173Asn
NM_005555.3:c.519G>T NP_005546.2:p.Lys173Asn
NM_005555.4:c.519G>T MANE Select NP_005546.2:p.Lys173Asn