Canonical Allele Identifier: CA1482797966
Gene:

Linked Data

dbSNP Id: rs1724787591

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542895G>A , CM000666.2:g.105542895G>A GRCh38
NC_000004.11:g.106464052G>A , CM000666.1:g.106464052G>A GRCh37
NC_000004.10:g.106683501G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-186C>T
XR_939039.1:n.456-186C>T
XR_939040.1:n.296-1419C>T
XR_001741410.1:n.311-186C>T
XR_001741411.1:n.787-186C>T
XR_001741412.1:n.311-186C>T
XR_001741413.1:n.311-186C>T
XR_001741414.1:n.311-186C>T
XR_939038.2:n.311-186C>T
XR_939040.2:n.311-1419C>T