Canonical Allele Identifier: CA8563386
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs748762166
ExAC: 17:39768963 G / A
gnomAD v2: 17-39768963-G-A
gnomAD v3: 17-41612711-G-A
gnomAD v4: 17-41612711-G-A
MyVariant Identifiers: chr17:g.39768963G>A (hg19) chr17:g.41612711G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612711G>A , CM000679.2:g.41612711G>A GRCh38
NC_000017.10:g.39768963G>A , CM000679.1:g.39768963G>A GRCh37
NC_000017.9:g.37022489G>A NCBI36
NG_008301.1:g.5117C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-23C>T MANE Select ENSP00000301653.3:n.-23C>T
ENST00000301653.8:c.-23C>T ENSP00000301653.3:n.-23C>T
ENST00000588319.1:n.55C>T
ENST00000590990.1:c.-23C>T ENSP00000467105.1:n.-23C>T
ENST00000593067.1:c.-313+79C>T ENSP00000467124.1:n.-313+79C>T
NM_005557.3:c.-23C>T NP_005548.2:n.-23C>T
NM_005557.4:c.-23C>T MANE Select NP_005548.2:n.-23C>T
Search 100 bp 5'
Search 100 bp 3'