Canonical Allele Identifier: CA1467350231
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743736C= , CM000666.2:g.71743736C= GRCh38
NC_000004.11:g.72609453C= , CM000666.1:g.72609453C= GRCh37
NC_000004.10:g.72828317C= NCBI36
NG_012837.2:g.66785G=
NG_012837.3:g.66785G=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-1866G= MANE Select ENSP00000273951.8:n.*26-1866G=
ENST00000273951.12:c.*26-1866G= ENSP00000273951.8:n.*26-1866G=
ENST00000503364.5:n.124-1866G=
ENST00000503472.5:n.1335-1866G=
ENST00000504199.5:c.*26-1866G= ENSP00000421725.1:n.*26-1866G=
ENST00000509740.5:c.*274-1866G= ENSP00000422664.1:n.*274-1866G=
ENST00000513476.5:c.1396-1866G= ENSP00000426683.1:n.1396-1866G=
NM_000583.3:c.*26-1866G= NP_000574.2:n.*26-1866G=
NM_001204306.1:c.*26-1866G= NP_001191235.1:n.*26-1866G=
NM_001204307.1:c.*26-1866G= NP_001191236.1:n.*26-1866G=
XM_006714177.2:c.*40-1866G= XP_006714240.1:n.*40-1866G=
XM_006714177.3:c.*40-1866G= XP_006714240.1:n.*40-1866G=
NM_000583.4:c.*26-1866G= MANE Select NP_000574.2:n.*26-1866G=