Canonical Allele Identifier: CA2637841154
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624580-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624580C>T , CM000679.2:g.41624580C>T GRCh38
NC_000017.10:g.39780832C>T , CM000679.1:g.39780832C>T GRCh37
NC_000017.9:g.37034358C>T NCBI36
NG_008625.1:g.5051G>A
NG_009090.2:g.167133G>A , LRG_401:g.167133G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463128.5:c.-313+163G>A ENSP00000468672.1:n.-313+163G>A
NM_000422.2:c.-71G>A NP_000413.1:n.-71G>A
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