Canonical Allele Identifier: CA2706722748
Gene:

Linked Data

dbSNP Id: rs2110368007

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542839T>C , CM000666.2:g.105542839T>C GRCh38
NC_000004.11:g.106463996T>C , CM000666.1:g.106463996T>C GRCh37
NC_000004.10:g.106683445T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-130A>G
XR_939039.1:n.456-130A>G
XR_939040.1:n.296-1363A>G
XR_001741410.1:n.311-130A>G
XR_001741411.1:n.787-130A>G
XR_001741412.1:n.311-130A>G
XR_001741413.1:n.311-130A>G
XR_001741414.1:n.311-130A>G
XR_939038.2:n.311-130A>G
XR_939040.2:n.311-1363A>G