Canonical Allele Identifier: CA649066102
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542896G>A , CM000666.2:g.105542896G>A GRCh38
NC_000004.11:g.106464053G>A , CM000666.1:g.106464053G>A GRCh37
NC_000004.10:g.106683502G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-187C>T
XR_939039.1:n.456-187C>T
XR_939040.1:n.296-1420C>T
XR_001741410.1:n.311-187C>T
XR_001741411.1:n.787-187C>T
XR_001741412.1:n.311-187C>T
XR_001741413.1:n.311-187C>T
XR_001741414.1:n.311-187C>T
XR_939038.2:n.311-187C>T
XR_939040.2:n.311-1420C>T