Canonical Allele Identifier: CA1066321262
Gene:

Linked Data

dbSNP Id: rs1724788861

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542966G>C , CM000666.2:g.105542966G>C GRCh38
NC_000004.11:g.106464123G>C , CM000666.1:g.106464123G>C GRCh37
NC_000004.10:g.106683572G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-257C>G
XR_939039.1:n.456-257C>G
XR_939040.1:n.296-1490C>G
XR_001741410.1:n.311-257C>G
XR_001741411.1:n.787-257C>G
XR_001741412.1:n.311-257C>G
XR_001741413.1:n.311-257C>G
XR_001741414.1:n.311-257C>G
XR_939038.2:n.311-257C>G
XR_939040.2:n.311-1490C>G