Canonical Allele Identifier: CA1912720761
Gene:

Linked Data

dbSNP Id: rs1839459560

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812584C>T , CM000672.2:g.57812584C>T GRCh38
NC_000010.10:g.59572344C>T , CM000672.1:g.59572344C>T GRCh37
NC_000010.9:g.59242350C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34708G>A
XR_001747454.1:n.85+34708G>A