Canonical Allele Identifier: CA1467350182
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs995981288

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743625G>T , CM000666.2:g.71743625G>T GRCh38
NC_000004.11:g.72609342G>T , CM000666.1:g.72609342G>T GRCh37
NC_000004.10:g.72828206G>T NCBI36
NG_012837.2:g.66896C>A
NG_012837.3:g.66896C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-1755C>A MANE Select ENSP00000273951.8:n.*26-1755C>A
ENST00000273951.12:c.*26-1755C>A ENSP00000273951.8:n.*26-1755C>A
ENST00000503364.5:n.124-1755C>A
ENST00000503472.5:n.1335-1755C>A
ENST00000504199.5:c.*26-1755C>A ENSP00000421725.1:n.*26-1755C>A
ENST00000509740.5:c.*274-1755C>A ENSP00000422664.1:n.*274-1755C>A
ENST00000513476.5:c.1396-1755C>A ENSP00000426683.1:n.1396-1755C>A
NM_000583.3:c.*26-1755C>A NP_000574.2:n.*26-1755C>A
NM_001204306.1:c.*26-1755C>A NP_001191235.1:n.*26-1755C>A
NM_001204307.1:c.*26-1755C>A NP_001191236.1:n.*26-1755C>A
XM_006714177.2:c.*40-1755C>A XP_006714240.1:n.*40-1755C>A
XM_006714177.3:c.*40-1755C>A XP_006714240.1:n.*40-1755C>A
NM_000583.4:c.*26-1755C>A MANE Select NP_000574.2:n.*26-1755C>A