Canonical Allele Identifier: CA1029770027
Gene:

Linked Data

dbSNP Id: rs1667992314
gnomAD v3: 2-41534725-A-G
gnomAD v4: 2-41534725-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534725A>G , CM000664.2:g.41534725A>G GRCh38
NC_000002.11:g.41761865A>G , CM000664.1:g.41761865A>G GRCh37
NC_000002.10:g.41615369A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3001T>C
XR_939997.1:n.146+3001T>C
XR_939997.2:n.9529+3001T>C