Canonical Allele Identifier: CA103381337
Gene:

Linked Data

dbSNP Id: rs6825245

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542960T>C , CM000666.2:g.105542960T>C GRCh38
NC_000004.11:g.106464117T>C , CM000666.1:g.106464117T>C GRCh37
NC_000004.10:g.106683566T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-251A>G
XR_939039.1:n.456-251A>G
XR_939040.1:n.296-1484A>G
XR_001741410.1:n.311-251A>G
XR_001741411.1:n.787-251A>G
XR_001741412.1:n.311-251A>G
XR_001741413.1:n.311-251A>G
XR_001741414.1:n.311-251A>G
XR_939038.2:n.311-251A>G
XR_939040.2:n.311-1484A>G