Canonical Allele Identifier: CA427349532
Gene:

Linked Data

gnomAD v3: 2-88016436-G-T
gnomAD v4: 2-88016436-G-T
MyVariant Identifiers: chr2:g.88315955G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016436G>T , CM000664.2:g.88016436G>T GRCh38
NC_000002.11:g.88315955G>T , CM000664.1:g.88315955G>T GRCh37
NC_000002.10:g.88097070G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.781G>T
XR_940336.3:n.781G>T