Canonical Allele Identifier: CA8563380
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs752063430
ExAC: 17:39768936 G / C
gnomAD v2: 17-39768936-G-C
gnomAD v4: 17-41612684-G-C
MyVariant Identifiers: chr17:g.39768936G>C (hg19) chr17:g.41612684G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612684G>C , CM000679.2:g.41612684G>C GRCh38
NC_000017.10:g.39768936G>C , CM000679.1:g.39768936G>C GRCh37
NC_000017.9:g.37022462G>C NCBI36
NG_008301.1:g.5144C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.5C>G MANE Select ENSP00000301653.3:p.Thr2Ser
ENST00000301653.8:c.5C>G ENSP00000301653.3:p.Thr2Ser
ENST00000588319.1:n.82C>G
ENST00000590990.1:c.5C>G ENSP00000467105.1:p.Thr2Ser
ENST00000593067.1:c.-313+106C>G ENSP00000467124.1:n.-313+106C>G
NM_005557.3:c.5C>G NP_005548.2:p.Thr2Ser
NM_005557.4:c.5C>G MANE Select NP_005548.2:p.Thr2Ser
Search 100 bp 5'
Search 100 bp 3'