Canonical Allele Identifier: CA1482797949
Gene:

Linked Data

dbSNP Id: rs1724787272

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542871A>G , CM000666.2:g.105542871A>G GRCh38
NC_000004.11:g.106464028A>G , CM000666.1:g.106464028A>G GRCh37
NC_000004.10:g.106683477A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-162T>C
XR_939039.1:n.456-162T>C
XR_939040.1:n.296-1395T>C
XR_001741410.1:n.311-162T>C
XR_001741411.1:n.787-162T>C
XR_001741412.1:n.311-162T>C
XR_001741413.1:n.311-162T>C
XR_001741414.1:n.311-162T>C
XR_939038.2:n.311-162T>C
XR_939040.2:n.311-1395T>C