Canonical Allele Identifier: CA2700552984
Gene:

Linked Data

dbSNP Id: rs2104988442

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431589G>T , CM000664.2:g.127431589G>T GRCh38
NC_000002.11:g.128189165G>T , CM000664.1:g.128189165G>T GRCh37
NC_000002.10:g.127905635G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923313.1:n.1331+78C>A
XR_001739705.1:n.3607-3325C>A
XR_923313.2:n.4042+78C>A