Canonical Allele Identifier: CA500206559
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908228487
gnomAD v3: 17-41612299-G-A
gnomAD v4: 17-41612299-G-A
MyVariant Identifiers: chr17:g.39768551G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612299G>A , CM000679.2:g.41612299G>A GRCh38
NC_000017.10:g.39768551G>A , CM000679.1:g.39768551G>A GRCh37
NC_000017.9:g.37022077G>A NCBI36
NG_008301.1:g.5529C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.390C>T MANE Select ENSP00000301653.3:p.Ser130=
ENST00000301653.8:c.390C>T ENSP00000301653.3:p.Ser130=
ENST00000588319.1:n.467C>T
ENST00000593067.1:c.-312-13C>T ENSP00000467124.1:n.-312-13C>T
NM_005557.3:c.390C>T NP_005548.2:p.Ser130=
NM_005557.4:c.390C>T MANE Select NP_005548.2:p.Ser130=
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Search 100 bp 3'