Canonical Allele Identifier: CA626016587
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs549505855
gnomAD v2: 17-39768361-C-G
gnomAD v4: 17-41612109-C-G
MyVariant Identifiers: chr17:g.39768361C>G (hg19) chr17:g.41612109C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612109C>G , CM000679.2:g.41612109C>G GRCh38
NC_000017.10:g.39768361C>G , CM000679.1:g.39768361C>G GRCh37
NC_000017.9:g.37021887C>G NCBI36
NG_008301.1:g.5719G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.531+49G>C MANE Select ENSP00000301653.3:n.531+49G>C
ENST00000301653.8:c.531+49G>C ENSP00000301653.3:n.531+49G>C
ENST00000588319.1:n.657G>C
ENST00000593067.1:c.-184+49G>C ENSP00000467124.1:n.-184+49G>C
NM_005557.3:c.531+49G>C NP_005548.2:n.531+49G>C
NM_005557.4:c.531+49G>C MANE Select NP_005548.2:n.531+49G>C
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