Canonical Allele Identifier: CA2809496615
Gene: KRT16 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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