Canonical Allele Identifier: CA2762952399
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542854T>C , CM000666.2:g.105542854T>C GRCh38
NC_000004.11:g.106464011T>C , CM000666.1:g.106464011T>C GRCh37
NC_000004.10:g.106683460T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-145A>G
XR_939039.1:n.456-145A>G
XR_939040.1:n.296-1378A>G
XR_001741410.1:n.311-145A>G
XR_001741411.1:n.787-145A>G
XR_001741412.1:n.311-145A>G
XR_001741413.1:n.311-145A>G
XR_001741414.1:n.311-145A>G
XR_939038.2:n.311-145A>G
XR_939040.2:n.311-1378A>G