Canonical Allele Identifier: CA16146337
Gene:

Linked Data

dbSNP Id: rs78518297
gnomAD v2: 3-70626309-T-C
gnomAD v3: 3-70577158-T-C
gnomAD v4: 3-70577158-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577158T>C , CM000665.2:g.70577158T>C GRCh38
NC_000003.11:g.70626309T>C , CM000665.1:g.70626309T>C GRCh37
NC_000003.10:g.70708999T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1205A>G
XR_001740559.1:n.367-1205A>G