Canonical Allele Identifier: CA2671644295
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542498A>G , CM000666.2:g.105542498A>G GRCh38
NC_000004.11:g.106463655A>G , CM000666.1:g.106463655A>G GRCh37
NC_000004.10:g.106683104A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.507T>C
XR_939039.1:n.667T>C
XR_939040.1:n.296-1022T>C
XR_001741410.1:n.522T>C
XR_001741411.1:n.998T>C
XR_001741412.1:n.449+73T>C
XR_001741413.1:n.522T>C
XR_001741414.1:n.449+73T>C
XR_939038.2:n.522T>C
XR_939040.2:n.311-1022T>C