Canonical Allele Identifier: CA244520175
Gene: HNF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1327601
ClinVar RCV Id: RCV001794545
dbSNP Id: rs970766228

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120978582C>T , CM000674.2:g.120978582C>T GRCh38
NC_000012.11:g.121416385C>T , CM000674.1:g.121416385C>T GRCh37
NC_000012.10:g.119900768C>T NCBI36
NG_011731.2:g.4837C>T , LRG_522:g.4837C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257555.11:c.-187C>T MANE Select ENSP00000257555.5:n.-187C>T
ENST00000257555.10:c.-187C>T ENSP00000257555.4:n.-187C>T
ENST00000400024.6:c.-187C>T ENSP00000476181.1:n.-187C>T
NM_000545.6:c.-187C>T NP_000536.5:n.-187C>T
NM_001306179.1:c.-187C>T NP_001293108.1:n.-187C>T
XM_005253931.2:c.-187C>T XP_005253988.1:n.-187C>T
XM_024449168.1:c.-187C>T XP_024304936.1:n.-187C>T
NM_000545.8:c.-187C>T MANE Select NP_000536.6:n.-187C>T
NM_001306179.2:c.-187C>T NP_001293108.2:n.-187C>T