Canonical Allele Identifier: CA2762952398
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542777A>C , CM000666.2:g.105542777A>C GRCh38
NC_000004.11:g.106463934A>C , CM000666.1:g.106463934A>C GRCh37
NC_000004.10:g.106683383A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-68T>G
XR_939039.1:n.456-68T>G
XR_939040.1:n.296-1301T>G
XR_001741410.1:n.311-68T>G
XR_001741411.1:n.787-68T>G
XR_001741412.1:n.311-68T>G
XR_001741413.1:n.311-68T>G
XR_001741414.1:n.311-68T>G
XR_939038.2:n.311-68T>G
XR_939040.2:n.311-1301T>G