Canonical Allele Identifier: CA427349480
Gene:

Linked Data

gnomAD v3: 2-88016411-G-T
gnomAD v4: 2-88016411-G-T
MyVariant Identifiers: chr2:g.88315930G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016411G>T , CM000664.2:g.88016411G>T GRCh38
NC_000002.11:g.88315930G>T , CM000664.1:g.88315930G>T GRCh37
NC_000002.10:g.88097045G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.756G>T
XR_940336.3:n.756G>T