Canonical Allele Identifier: CA2671644324
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542815A>G , CM000666.2:g.105542815A>G GRCh38
NC_000004.11:g.106463972A>G , CM000666.1:g.106463972A>G GRCh37
NC_000004.10:g.106683421A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-106T>C
XR_939039.1:n.456-106T>C
XR_939040.1:n.296-1339T>C
XR_001741410.1:n.311-106T>C
XR_001741411.1:n.787-106T>C
XR_001741412.1:n.311-106T>C
XR_001741413.1:n.311-106T>C
XR_001741414.1:n.311-106T>C
XR_939038.2:n.311-106T>C
XR_939040.2:n.311-1339T>C