Canonical Allele Identifier: CA1218511474
Gene:

Linked Data

dbSNP Id: rs1658967624

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198499990A>C , CM000663.2:g.198499990A>C GRCh38
NC_000001.10:g.198469120A>C , CM000663.1:g.198469120A>C GRCh37
NC_000001.9:g.196735743A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922398.1:n.679+19561T>G
XR_922398.2:n.341+19561T>G