Canonical Allele Identifier: CA2700110959
Gene:

Linked Data

dbSNP Id: rs1356741343

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079689T>G , CM000664.2:g.118079689T>G GRCh38
NC_000002.11:g.118837265T>G , CM000664.1:g.118837265T>G GRCh37
NC_000002.10:g.118553735T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2157A>C XP_011510607.1:n.697-2157A>C
XR_001739662.2:n.138+8562A>C