Canonical Allele Identifier: CA2721793270
Gene:

Linked Data

dbSNP Id: rs2132201011

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812963A>T , CM000672.2:g.57812963A>T GRCh38
NC_000010.10:g.59572723A>T , CM000672.1:g.59572723A>T GRCh37
NC_000010.9:g.59242729A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34329T>A
XR_001747454.1:n.85+34329T>A