Canonical Allele Identifier: CA784842251
Gene:

Linked Data

dbSNP Id: rs1192996296

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542499G>A , CM000666.2:g.105542499G>A GRCh38
NC_000004.11:g.106463656G>A , CM000666.1:g.106463656G>A GRCh37
NC_000004.10:g.106683105G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.506C>T
XR_939039.1:n.666C>T
XR_939040.1:n.296-1023C>T
XR_001741410.1:n.521C>T
XR_001741411.1:n.997C>T
XR_001741412.1:n.449+72C>T
XR_001741413.1:n.521C>T
XR_001741414.1:n.449+72C>T
XR_939038.2:n.521C>T
XR_939040.2:n.311-1023C>T