Canonical Allele Identifier: CA101090329
Gene:

Linked Data

dbSNP Id: rs4693646
gnomAD v2: 4-84721814-A-G
gnomAD v3: 4-83800661-A-G
gnomAD v4: 4-83800661-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.83800661A>G , CM000666.2:g.83800661A>G GRCh38
NC_000004.11:g.84721814A>G , CM000666.1:g.84721814A>G GRCh37
NC_000004.10:g.84940838A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938946.1:n.80+2088T>C
XR_938946.2:n.80+2088T>C