Canonical Allele Identifier: CA2260099970
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612769G= , CM000679.2:g.41612769G= GRCh38
NC_000017.10:g.39769021G= , CM000679.1:g.39769021G= GRCh37
NC_000017.9:g.37022547G= NCBI36
NG_008301.1:g.5059C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000590990.1:c.-36-45C= ENSP00000467105.1:n.-36-45C=
ENST00000593067.1:c.-313+21C= ENSP00000467124.1:n.-313+21C=
NM_005557.3:c.-81C= NP_005548.2:n.-81C=