Canonical Allele Identifier: CA1482797548
Gene:

Linked Data

dbSNP Id: rs1724780839

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542569A>G , CM000666.2:g.105542569A>G GRCh38
NC_000004.11:g.106463726A>G , CM000666.1:g.106463726A>G GRCh37
NC_000004.10:g.106683175A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.436T>C
XR_939039.1:n.596T>C
XR_939040.1:n.296-1093T>C
XR_001741410.1:n.451T>C
XR_001741411.1:n.927T>C
XR_001741412.1:n.449+2T>C
XR_001741413.1:n.451T>C
XR_001741414.1:n.449+2T>C
XR_939038.2:n.451T>C
XR_939040.2:n.311-1093T>C