Canonical Allele Identifier: CA8563263
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs763404327
ExAC: 17:39768473 C / G
gnomAD v2: 17-39768473-C-G
MyVariant Identifiers: chr17:g.39768473C>G (hg19) chr17:g.41612221C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612221C>G , CM000679.2:g.41612221C>G GRCh38
NC_000017.10:g.39768473C>G , CM000679.1:g.39768473C>G GRCh37
NC_000017.9:g.37021999C>G NCBI36
NG_008301.1:g.5607G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.468G>C MANE Select ENSP00000301653.3:p.Gln156His
ENST00000301653.8:c.468G>C ENSP00000301653.3:p.Gln156His
ENST00000588319.1:n.545G>C
ENST00000593067.1:c.-247G>C ENSP00000467124.1:n.-247G>C
NM_005557.3:c.468G>C NP_005548.2:p.Gln156His
NM_005557.4:c.468G>C MANE Select NP_005548.2:p.Gln156His
Search 100 bp 5'
Search 100 bp 3'