Canonical Allele Identifier: CA1104780658
Gene:

Linked Data

dbSNP Id: rs1789258588
gnomAD v3: 7-97388615-C-G
gnomAD v4: 7-97388615-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388615C>G , CM000669.2:g.97388615C>G GRCh38
NC_000007.13:g.97017927C>G , CM000669.1:g.97017927C>G GRCh37
NC_000007.12:g.96855863C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59968G>C