Canonical Allele Identifier: CA735545612
Gene:

Linked Data

dbSNP Id: rs934521626

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38168059G>T , CM000663.2:g.38168059G>T GRCh38
NC_000001.10:g.38633731G>T , CM000663.1:g.38633731G>T GRCh37
NC_000001.9:g.38406318G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947202.1:n.175+6236G>T
XR_947203.1:n.62-24946G>T
XR_947204.1:n.175+6236G>T
XR_947205.1:n.175+6236G>T
XR_001737984.1:n.175+6236G>T
XR_001737985.1:n.62-24946G>T
XR_001737986.1:n.175+6236G>T
XR_001737987.1:n.175+6236G>T
XR_002958294.1:n.175+6236G>T
XR_947205.2:n.175+6236G>T