Canonical Allele Identifier: CA1912720905
Gene:

Linked Data

dbSNP Id: rs1589010481

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812863T>A , CM000672.2:g.57812863T>A GRCh38
NC_000010.10:g.59572623T>A , CM000672.1:g.59572623T>A GRCh37
NC_000010.9:g.59242629T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34429A>T
XR_001747454.1:n.85+34429A>T