Canonical Allele Identifier: CA8563909
Gene: KRT17 HGNC NCBI

Linked Data

dbSNP Id: rs149859406
ExAC: 17:39780804 G / C
gnomAD v2: 17-39780804-G-C
gnomAD v4: 17-41624552-G-C
MyVariant Identifiers: chr17:g.39780804G>C (hg19) chr17:g.41624552G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624552G>C , CM000679.2:g.41624552G>C GRCh38
NC_000017.10:g.39780804G>C , CM000679.1:g.39780804G>C GRCh37
NC_000017.9:g.37034330G>C NCBI36
NG_008625.1:g.5079C>G
NG_009090.2:g.167161C>G , LRG_401:g.167161C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-43C>G MANE Select ENSP00000308452.8:n.-43C>G
ENST00000311208.12:c.-43C>G ENSP00000308452.8:n.-43C>G
ENST00000463128.5:c.-313+191C>G ENSP00000468672.1:n.-313+191C>G
ENST00000491673.1:n.24C>G
NM_000422.2:c.-43C>G NP_000413.1:n.-43C>G
NM_000422.3:c.-43C>G MANE Select NP_000413.1:n.-43C>G
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