Canonical Allele Identifier: CA99066909
Gene: GC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10488854

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71758418C>T , CM000666.2:g.71758418C>T GRCh38
NC_000004.11:g.72624135C>T , CM000666.1:g.72624135C>T GRCh37
NC_000004.10:g.72842999C>T NCBI36
NG_012837.2:g.52103G>A

Transcript Alleles

HGVS Amino-acid change
NM_000583.3:c.702-247G>A VV NP_000574.2:p.=
NM_001204306.1:c.702-247G>A VV NP_001191235.1:p.=
NM_001204307.1:c.759-247G>A VV NP_001191236.1:p.=
XM_006714177.2:c.702-247G>A XP_006714240.1:p.=
XM_006714177.3:c.702-247G>A
ENST00000273951.12:c.702-247G>A ENSP00000273951.8:p.=
ENST00000503472.5:n.586-247G>A
ENST00000504199.5:c.759-247G>A ENSP00000421725.1:p.=
ENST00000509740.5:c.702-247G>A ENSP00000422664.1:p.=
ENST00000513476.5:c.702-247G>A ENSP00000426683.1:p.=