Canonical Allele Identifier: CA8563237
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs766744891
ExAC: 17:39768364 T / G
gnomAD v2: 17-39768364-T-G
gnomAD v3: 17-41612112-T-G
gnomAD v4: 17-41612112-T-G
MyVariant Identifiers: chr17:g.39768364T>G (hg19) chr17:g.41612112T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612112T>G , CM000679.2:g.41612112T>G GRCh38
NC_000017.10:g.39768364T>G , CM000679.1:g.39768364T>G GRCh37
NC_000017.9:g.37021890T>G NCBI36
NG_008301.1:g.5716A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.531+46A>C MANE Select ENSP00000301653.3:n.531+46A>C
ENST00000301653.8:c.531+46A>C ENSP00000301653.3:n.531+46A>C
ENST00000588319.1:n.654A>C
ENST00000593067.1:c.-184+46A>C ENSP00000467124.1:n.-184+46A>C
NM_005557.3:c.531+46A>C NP_005548.2:n.531+46A>C
NM_005557.4:c.531+46A>C MANE Select NP_005548.2:n.531+46A>C
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