Canonical Allele Identifier: CA1033291273

Gene:

Linked Data

• dbSNP Id: rs7603671
• gnomAD v3: 2-88016302-G-T
• gnomAD v4: 2-88016302-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016302G>T , CM000664.2:g.88016302G>T	GRCh38
NC_000002.11:g.88315821G>T , CM000664.1:g.88315821G>T	GRCh37
NC_000002.10:g.88096936G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.647G>T
XR_940336.3:n.647G>T