Canonical Allele Identifier: CA8563322
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs772429436

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612496C>G , CM000679.2:g.41612496C>G GRCh38
NC_000017.10:g.39768748C>G , CM000679.1:g.39768748C>G GRCh37
NC_000017.9:g.37022274C>G NCBI36
NG_008301.1:g.5332G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.193G>C MANE Select ENSP00000301653.3:p.Gly65Arg
ENST00000301653.8:c.193G>C ENSP00000301653.3:p.Gly65Arg
ENST00000588319.1:n.270G>C
ENST00000593067.1:c.-312-210G>C ENSP00000467124.1:n.-312-210G>C
NM_005557.3:c.193G>C NP_005548.2:p.Gly65Arg
NM_005557.4:c.193G>C MANE Select NP_005548.2:p.Gly65Arg