Canonical Allele Identifier: CA764687408

Linked Data

dbSNP Id: rs1330410699

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033985C>G , CM000664.2:g.216033985C>G GRCh38
NC_000002.11:g.216898708C>G , CM000664.1:g.216898708C>G GRCh37
NC_000002.10:g.216606953C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424992.5:c.-91G>C (MREG) ENSP00000413302.1:n.-91G>C
ENST00000442122.5:c.*440+5206G>C (PECR) ENSP00000395512.1:n.*440+5206G>C
XR_001738847.2:n.1056-1133G>C (PECR)
NM_001372189.1:c.-91G>C (MREG) NP_001359118.1:n.-91G>C