Canonical Allele Identifier: CA13334273
Gene:

Linked Data

dbSNP Id: rs7913069

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103954641C>T , CM000672.2:g.103954641C>T GRCh38
NC_000010.10:g.105714399C>T , CM000672.1:g.105714399C>T GRCh37
NC_000010.9:g.105704389C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428807.2:n.389+5122G>A
XR_946276.1:n.393+5122G>A
XR_946277.1:n.393+5122G>A
XR_946278.1:n.503+5122G>A
XR_946279.1:n.522+5122G>A
XR_946280.1:n.389+5122G>A
XR_946281.1:n.306+5122G>A
XR_001747579.1:n.614+3818G>A
XR_428807.3:n.393+5122G>A
XR_946280.2:n.393+5122G>A