Canonical Allele Identifier: CA1912720938
Gene:

Linked Data

dbSNP Id: rs1589010504

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812936C>A , CM000672.2:g.57812936C>A GRCh38
NC_000010.10:g.59572696C>A , CM000672.1:g.59572696C>A GRCh37
NC_000010.9:g.59242702C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34356G>T
XR_001747454.1:n.85+34356G>T