Canonical Allele Identifier: CA1467353650
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71751269G= , CM000666.2:g.71751269G= GRCh38
NC_000004.11:g.72616986G= , CM000666.1:g.72616986G= GRCh37
NC_000004.10:g.72835850G= NCBI36
NG_012837.2:g.59252C=
NG_012837.3:g.59252C=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1395+1249C= MANE Select ENSP00000273951.8:n.1395+1249C=
ENST00000273951.12:c.1395+1249C= ENSP00000273951.8:n.1395+1249C=
ENST00000503364.5:n.68+3142C=
ENST00000503472.5:n.1279+1249C=
ENST00000504199.5:c.1452+1249C= ENSP00000421725.1:n.1452+1249C=
ENST00000509740.5:c.*218+1249C= ENSP00000422664.1:n.*218+1249C=
ENST00000513476.5:c.1395+1249C= ENSP00000426683.1:n.1395+1249C=
NM_000583.3:c.1395+1249C= NP_000574.2:n.1395+1249C=
NM_001204306.1:c.1395+1249C= NP_001191235.1:n.1395+1249C=
NM_001204307.1:c.1452+1249C= NP_001191236.1:n.1452+1249C=
XM_006714177.2:c.1262+3142C= XP_006714240.1:n.1262+3142C=
XM_006714177.3:c.1262+3142C= XP_006714240.1:n.1262+3142C=
NM_000583.4:c.1395+1249C= MANE Select NP_000574.2:n.1395+1249C=