Canonical Allele Identifier: CA2700222259
Gene:

Linked Data

dbSNP Id: rs2104511492

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079669G>C , CM000664.2:g.118079669G>C GRCh38
NC_000002.11:g.118837245G>C , CM000664.1:g.118837245G>C GRCh37
NC_000002.10:g.118553715G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2137C>G XP_011510607.1:n.697-2137C>G
XR_001739662.2:n.138+8582C>G