Canonical Allele Identifier: CA2260099589
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908220484
gnomAD v4: 17-41612108-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612108C>T , CM000679.2:g.41612108C>T GRCh38
NC_000017.10:g.39768360C>T , CM000679.1:g.39768360C>T GRCh37
NC_000017.9:g.37021886C>T NCBI36
NG_008301.1:g.5720G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.531+50G>A MANE Select ENSP00000301653.3:n.531+50G>A
ENST00000301653.8:c.531+50G>A ENSP00000301653.3:n.531+50G>A
ENST00000588319.1:n.658G>A
ENST00000593067.1:c.-184+50G>A ENSP00000467124.1:n.-184+50G>A
NM_005557.3:c.531+50G>A NP_005548.2:n.531+50G>A
NM_005557.4:c.531+50G>A MANE Select NP_005548.2:n.531+50G>A
Search 100 bp 5'
Search 100 bp 3'