Canonical Allele Identifier: CA2260099969
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612768G= , CM000679.2:g.41612768G= GRCh38
NC_000017.10:g.39769020G= , CM000679.1:g.39769020G= GRCh37
NC_000017.9:g.37022546G= NCBI36
NG_008301.1:g.5060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000590990.1:c.-36-44C= ENSP00000467105.1:n.-36-44C=
ENST00000593067.1:c.-313+22C= ENSP00000467124.1:n.-313+22C=
NM_005557.3:c.-80C= NP_005548.2:n.-80C=