Canonical Allele Identifier: CA15438622
Gene: C2 HGNC NCBI

Linked Data

dbSNP Id: rs558702
gnomAD v2: 6-31870326-G-A
gnomAD v3: 6-31902549-G-A
gnomAD v4: 6-31902549-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31902549G>A , CM000668.2:g.31902549G>A GRCh38
NC_000006.11:g.31870326G>A , CM000668.1:g.31870326G>A GRCh37
NC_000006.10:g.31978305G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452323.7:c.73+1410G>A ENSP00000392322.2:n.73+1410G>A
ENST00000497706.6:c.-64+4607G>A ENSP00000417482.2:n.-64+4607G>A
ENST00000695637.1:c.-360+4274G>A ENSP00000512074.1:n.-360+4274G>A
ENST00000452202.5:c.73+1410G>A ENSP00000406121.1:n.73+1410G>A
ENST00000452323.6:c.73+1410G>A ENSP00000392322.2:n.73+1410G>A
ENST00000469372.5:c.-64+4607G>A ENSP00000418923.1:n.-64+4607G>A
ENST00000497706.5:c.-64+4607G>A ENSP00000417482.1:n.-64+4607G>A
NM_001178063.2:c.73+1410G>A NP_001171534.1:n.73+1410G>A
NM_001282457.1:c.-64+4607G>A NP_001269386.1:n.-64+4607G>A
NM_001282457.2:c.-64+4607G>A NP_001269386.1:n.-64+4607G>A
NM_001178063.3:c.73+1410G>A NP_001171534.1:n.73+1410G>A