Canonical Allele Identifier: CA772032782
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs1318951793
gnomAD v3: 17-41624578-G-A
gnomAD v4: 17-41624578-G-A
MyVariant Identifiers: chr17:g.39780830G>A (hg19) chr17:g.41624578G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624578G>A , CM000679.2:g.41624578G>A GRCh38
NC_000017.10:g.39780830G>A , CM000679.1:g.39780830G>A GRCh37
NC_000017.9:g.37034356G>A NCBI36
NG_008625.1:g.5053C>T
NG_009090.2:g.167135C>T , LRG_401:g.167135C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463128.5:c.-313+165C>T ENSP00000468672.1:n.-313+165C>T
NM_000422.2:c.-69C>T NP_000413.1:n.-69C>T
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