Canonical Allele Identifier: CA41586372
Gene:

Linked Data

dbSNP Id: rs573454645
gnomAD v2: 2-773329-C-G
gnomAD v3: 2-773329-C-G
gnomAD v4: 2-773329-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773329C>G , CM000664.2:g.773329C>G GRCh38
NC_000002.11:g.773329C>G , CM000664.1:g.773329C>G GRCh37
NC_000002.10:g.763329C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510439.1:c.-24-3507C>G XP_011508741.1:n.-24-3507C>G
XM_011510440.1:c.-24-3507C>G XP_011508742.1:n.-24-3507C>G
XM_011510441.1:c.-24-3507C>G XP_011508743.1:n.-24-3507C>G
XM_011510442.1:c.-24-3507C>G XP_011508744.1:n.-24-3507C>G
XM_011510443.1:c.-24-3507C>G XP_011508745.1:n.-24-3507C>G
XR_922708.1:n.4001-3507C>G