Canonical Allele Identifier: CA1482797943
Gene:

Linked Data

dbSNP Id: rs1578237049

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542869G>A , CM000666.2:g.105542869G>A GRCh38
NC_000004.11:g.106464026G>A , CM000666.1:g.106464026G>A GRCh37
NC_000004.10:g.106683475G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-160C>T
XR_939039.1:n.456-160C>T
XR_939040.1:n.296-1393C>T
XR_001741410.1:n.311-160C>T
XR_001741411.1:n.787-160C>T
XR_001741412.1:n.311-160C>T
XR_001741413.1:n.311-160C>T
XR_001741414.1:n.311-160C>T
XR_939038.2:n.311-160C>T
XR_939040.2:n.311-1393C>T