Canonical Allele Identifier: CA2637841085
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624577-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624577G>T , CM000679.2:g.41624577G>T GRCh38
NC_000017.10:g.39780829G>T , CM000679.1:g.39780829G>T GRCh37
NC_000017.9:g.37034355G>T NCBI36
NG_008625.1:g.5054C>A
NG_009090.2:g.167136C>A , LRG_401:g.167136C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.12:c.-68C>A ENSP00000308452.8:n.-68C>A
ENST00000463128.5:c.-313+166C>A ENSP00000468672.1:n.-313+166C>A
NM_000422.2:c.-68C>A NP_000413.1:n.-68C>A
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