Canonical Allele Identifier: CA2260099971

Gene: KRT16

Linked Data

• dbSNP Id: rs989588698
• gnomAD v4: 17-41612769-G-C

Genomic Alleles

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

Transcript Alleles

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