Canonical Allele Identifier: CA2830591688

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542941A>G , CM000666.2:g.105542941A>G	GRCh38
NC_000004.11:g.106464098A>G , CM000666.1:g.106464098A>G	GRCh37
NC_000004.10:g.106683547A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.296-232T>C
XR_939039.1:n.456-232T>C
XR_939040.1:n.296-1465T>C
XR_001741410.1:n.311-232T>C
XR_001741411.1:n.787-232T>C
XR_001741412.1:n.311-232T>C
XR_001741413.1:n.311-232T>C
XR_001741414.1:n.311-232T>C
XR_939038.2:n.311-232T>C
XR_939040.2:n.311-1465T>C