Canonical Allele Identifier: CA772024463
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1331768419
gnomAD v3: 17-41612763-G-T
gnomAD v4: 17-41612763-G-T
MyVariant Identifiers: chr17:g.39769015G>T (hg19) chr17:g.41612763G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612763G>T , CM000679.2:g.41612763G>T GRCh38
NC_000017.10:g.39769015G>T , CM000679.1:g.39769015G>T GRCh37
NC_000017.9:g.37022541G>T NCBI36
NG_008301.1:g.5065C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-75C>A MANE Select ENSP00000301653.3:n.-75C>A
ENST00000588319.1:n.3C>A
ENST00000590990.1:c.-36-39C>A ENSP00000467105.1:n.-36-39C>A
ENST00000593067.1:c.-313+27C>A ENSP00000467124.1:n.-313+27C>A
NM_005557.3:c.-75C>A NP_005548.2:n.-75C>A
NM_005557.4:c.-75C>A MANE Select NP_005548.2:n.-75C>A
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