Canonical Allele Identifier: CA2706722196
Gene:

Linked Data

dbSNP Id: rs2110367714

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542552A>G , CM000666.2:g.105542552A>G GRCh38
NC_000004.11:g.106463709A>G , CM000666.1:g.106463709A>G GRCh37
NC_000004.10:g.106683158A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.453T>C
XR_939039.1:n.613T>C
XR_939040.1:n.296-1076T>C
XR_001741410.1:n.468T>C
XR_001741411.1:n.944T>C
XR_001741412.1:n.449+19T>C
XR_001741413.1:n.468T>C
XR_001741414.1:n.449+19T>C
XR_939038.2:n.468T>C
XR_939040.2:n.311-1076T>C