Canonical Allele Identifier: CA573583321
Gene:

Linked Data

dbSNP Id: rs1363122280
gnomAD v2: 7-26645372-A-G
gnomAD v3: 7-26605753-A-G
gnomAD v4: 7-26605753-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605753A>G , CM000669.2:g.26605753A>G GRCh38
NC_000007.13:g.26645372A>G , CM000669.1:g.26645372A>G GRCh37
NC_000007.12:g.26611897A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6383T>C
XR_927131.2:n.1186-6383T>C