Canonical Allele Identifier: CA936775737

Gene:

Linked Data

• dbSNP Id: rs1851770464
• gnomAD v3: 11-34812230-A-G
• gnomAD v4: 11-34812230-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812230A>G , CM000673.2:g.34812230A>G	GRCh38
NC_000011.9:g.34833777A>G , CM000673.1:g.34833777A>G	GRCh37
NC_000011.8:g.34790353A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57623A>G
XR_931188.1:n.693+57623A>G
XR_931189.1:n.854+57623A>G
XR_931190.1:n.639+57623A>G
XR_931191.1:n.689+57623A>G
XR_001748174.1:n.855+57623A>G
XR_001748176.1:n.1016+57623A>G
XR_002957246.1:n.639+57623A>G