Canonical Allele Identifier: CA8563256
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs771047238
ExAC: 17:39768448 T / G
gnomAD v2: 17-39768448-T-G
gnomAD v3: 17-41612196-T-G
gnomAD v4: 17-41612196-T-G
MyVariant Identifiers: chr17:g.39768448T>G (hg19) chr17:g.41612196T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612196T>G , CM000679.2:g.41612196T>G GRCh38
NC_000017.10:g.39768448T>G , CM000679.1:g.39768448T>G GRCh37
NC_000017.9:g.37021974T>G NCBI36
NG_008301.1:g.5632A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.493A>C MANE Select ENSP00000301653.3:p.Ser165Arg
ENST00000301653.8:c.493A>C ENSP00000301653.3:p.Ser165Arg
ENST00000588319.1:n.570A>C
ENST00000593067.1:c.-222A>C ENSP00000467124.1:n.-222A>C
NM_005557.3:c.493A>C NP_005548.2:p.Ser165Arg
NM_005557.4:c.493A>C MANE Select NP_005548.2:p.Ser165Arg
Search 100 bp 5'
Search 100 bp 3'