Canonical Allele Identifier: CA244520152
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1342947
dbSNP Id: rs756136537

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120978511A>G , CM000674.2:g.120978511A>G GRCh38
NC_000012.11:g.121416314A>G , CM000674.1:g.121416314A>G GRCh37
NC_000012.10:g.119900697A>G NCBI36
NG_011731.2:g.4766A>G , LRG_522:g.4766A>G

Transcript Alleles

HGVS Amino-acid Change
XM_005253931.2:c.-258A>G XP_005253988.1:n.-258A>G
XM_024449168.1:c.-258A>G XP_024304936.1:n.-258A>G