Canonical Allele Identifier: CA1482798025
Gene:

Linked Data

dbSNP Id: rs1724788628

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542959T>C , CM000666.2:g.105542959T>C GRCh38
NC_000004.11:g.106464116T>C , CM000666.1:g.106464116T>C GRCh37
NC_000004.10:g.106683565T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-250A>G
XR_939039.1:n.456-250A>G
XR_939040.1:n.296-1483A>G
XR_001741410.1:n.311-250A>G
XR_001741411.1:n.787-250A>G
XR_001741412.1:n.311-250A>G
XR_001741413.1:n.311-250A>G
XR_001741414.1:n.311-250A>G
XR_939038.2:n.311-250A>G
XR_939040.2:n.311-1483A>G