Canonical Allele Identifier: CA399496196
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1385661935
gnomAD v2: 17-39768780-G-T
gnomAD v4: 17-41612528-G-T
MyVariant Identifiers: chr17:g.39768780G>T (hg19) chr17:g.41612528G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612528G>T , CM000679.2:g.41612528G>T GRCh38
NC_000017.10:g.39768780G>T , CM000679.1:g.39768780G>T GRCh37
NC_000017.9:g.37022306G>T NCBI36
NG_008301.1:g.5300C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.161C>A MANE Select ENSP00000301653.3:p.Ser54Tyr
ENST00000301653.8:c.161C>A ENSP00000301653.3:p.Ser54Tyr
ENST00000588319.1:n.238C>A
ENST00000593067.1:c.-312-242C>A ENSP00000467124.1:n.-312-242C>A
NM_005557.3:c.161C>A NP_005548.2:p.Ser54Tyr
NM_005557.4:c.161C>A MANE Select NP_005548.2:p.Ser54Tyr
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