Canonical Allele Identifier: CA6142395
Gene: CABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67519905G>C , CM000673.2:g.67519905G>C GRCh38
NC_000011.9:g.67287376G>C , CM000673.1:g.67287376G>C GRCh37
NC_000011.8:g.67043952G>C NCBI36
NG_032982.1:g.8524C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000294288.5:c.525C>G MANE Select ENSP00000294288.4:p.Gly175=
ENST00000545205.2:c.*310C>G ENSP00000446180.1:n.*310C>G
ENST00000636477.1:c.477C>G ENSP00000490746.1:p.Gly159=
ENST00000294288.4:c.525C>G ENSP00000294288.4:p.Gly175=
ENST00000353903.9:c.354C>G ENSP00000312037.4:p.Gly118=
ENST00000545205.1:c.*310C>G ENSP00000446180.1:n.*310C>G
NM_016366.2:c.525C>G NP_057450.2:p.Gly175=
XM_005274046.1:c.543C>G XP_005274103.1:p.Gly181=
NM_001318496.1:c.543C>G NP_001305425.1:p.Gly181=
NM_001318496.2:c.543C>G NP_001305425.1:p.Gly181=
NM_016366.3:c.525C>G MANE Select NP_057450.2:p.Gly175=