Canonical Allele Identifier: CA692802475
Gene:

Linked Data

dbSNP Id: rs1240034455
gnomAD v3: 12-84951890-G-T
gnomAD v4: 12-84951890-G-T
MyVariant Identifiers: chr12:g.85345669G>T (hg19) chr12:g.84951890G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84951890G>T , CM000674.2:g.84951890G>T GRCh38
NC_000012.11:g.85345669G>T , CM000674.1:g.85345669G>T GRCh37
NC_000012.10:g.83869800G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30576G>T
XR_945153.1:n.301+13426G>T
XR_945154.1:n.174+37028G>T
XR_945155.1:n.330+30576G>T
XR_945152.2:n.316+30576G>T
XR_945154.2:n.174+37028G>T
XR_945155.2:n.888+30576G>T
Search 100 bp 5'
Search 100 bp 3'