Canonical Allele Identifier: CA1315898055
Gene: C2orf88 HGNC NCBI

Linked Data

dbSNP Id: rs1687225057
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190121004T>G , CM000664.2:g.190121004T>G GRCh38
NC_000002.11:g.190985730T>G , CM000664.1:g.190985730T>G GRCh37
NC_000002.10:g.190693975T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450357.5:c.-290+30034T>G ENSP00000394370.1:n.-290+30034T>G
ENST00000490033.5:n.226+25402T>G
ENST00000495546.1:n.271+40981T>G
XM_005246905.1:c.-290+40981T>G XP_005246962.1:n.-290+40981T>G
XM_011511982.1:c.-290+30034T>G XP_011510284.1:n.-290+30034T>G
XM_011511983.1:c.-290+25402T>G XP_011510285.1:n.-290+25402T>G
XM_011511984.1:c.-290+25402T>G XP_011510286.1:n.-290+25402T>G
XM_011511985.1:c.-290+30034T>G XP_011510287.1:n.-290+30034T>G
XM_011511986.1:c.-165+40981T>G XP_011510288.1:n.-165+40981T>G
XM_011511984.3:c.-290+25402T>G XP_011510286.1:n.-290+25402T>G
XM_011511985.3:c.-290+30034T>G XP_011510287.1:n.-290+30034T>G
XM_011511986.2:c.-165+40981T>G XP_011510288.1:n.-165+40981T>G
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