Canonical Allele Identifier: CA569179914
Gene:

Linked Data

dbSNP Id: rs1276095617
gnomAD v2: 6-98462583-A-C
gnomAD v3: 6-98014707-A-C
gnomAD v4: 6-98014707-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014707A>C , CM000668.2:g.98014707A>C GRCh38
NC_000006.11:g.98462583A>C , CM000668.1:g.98462583A>C GRCh37
NC_000006.10:g.98569304A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45241A>C
XR_942809.1:n.371+45241A>C