Canonical Allele Identifier: CA16620406
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 419351
ClinVar RCV Id: RCV000478068
dbSNP Id: rs28928894
MyVariant Identifiers: chr17:g.39768579A>C (hg19) chr17:g.41612327A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612327A>C , CM000679.2:g.41612327A>C GRCh38
NC_000017.10:g.39768579A>C , CM000679.1:g.39768579A>C GRCh37
NC_000017.9:g.37022105A>C NCBI36
NG_008301.1:g.5501T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.362T>G MANE Select ENSP00000301653.3:p.Met121Arg
ENST00000301653.8:c.362T>G ENSP00000301653.3:p.Met121Arg
ENST00000588319.1:n.439T>G
ENST00000593067.1:c.-312-41T>G ENSP00000467124.1:n.-312-41T>G
NM_005557.3:c.362T>G NP_005548.2:p.Met121Arg
NM_005557.4:c.362T>G MANE Select NP_005548.2:p.Met121Arg
Search 100 bp 5'
Search 100 bp 3'