Canonical Allele Identifier: CA15360577
Gene: GC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2298850

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71748550G>C , CM000666.2:g.71748550G>C GRCh38
NC_000004.11:g.72614267G>C , CM000666.1:g.72614267G>C GRCh37
NC_000004.10:g.72833131G>C NCBI36
NG_012837.2:g.61971C>G
NG_012837.3:g.61971C>G

Transcript Alleles

HGVS Amino-acid change
NM_000583.3:c.1396-2345C>G VV NP_000574.2:p.=
NM_001204306.1:c.1396-2345C>G VV NP_001191235.1:p.=
NM_001204307.1:c.1453-2345C>G VV NP_001191236.1:p.=
XM_006714177.2:c.1263-2345C>G XP_006714240.1:p.=
XM_006714177.3:c.1263-2345C>G
NM_000583.4:c.1396-2345C>G VV MANE Preferred
ENST00000273951.12:c.1396-2345C>G ENSP00000273951.8:p.=
ENST00000503364.5:n.69-2345C>G
ENST00000503472.5:n.1280-2345C>G
ENST00000504199.5:c.1453-2345C>G ENSP00000421725.1:p.=
ENST00000509740.5:c.*219-2345C>G ENSP00000422664.1:p.=
ENST00000513476.5:c.1395+3968C>G ENSP00000426683.1:p.=