Canonical Allele Identifier: CA11112125
Gene:

Linked Data

dbSNP Id: rs1839158
gnomAD v2: 2-33855431-C-G
gnomAD v3: 2-33630364-C-G
gnomAD v4: 2-33630364-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33630364C>G , CM000664.2:g.33630364C>G GRCh38
NC_000002.11:g.33855431C>G , CM000664.1:g.33855431C>G GRCh37
NC_000002.10:g.33708935C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939941.1:n.227-2247C>G
XR_939942.1:n.227-21949C>G
XR_939943.1:n.97-2247C>G
XR_939941.2:n.236-2247C>G
XR_939942.2:n.236-21949C>G