Canonical Allele Identifier: CA798110183

Gene: GC

Linked Data

• dbSNP Id: rs1321716116
• MyVariant Identifiers: chr4:g.72621291T>C (hg19) ; chr4:g.71755574T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755574T>C , CM000666.2:g.71755574T>C	GRCh38
NC_000004.11:g.72621291T>C , CM000666.1:g.72621291T>C	GRCh37
NC_000004.10:g.72840155T>C	NCBI36
NG_012837.2:g.54947A>G
NG_012837.3:g.54947A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-467A>G MANE Select	ENSP00000273951.8:n.1035-467A>G
ENST00000273951.12:c.1035-467A>G	ENSP00000273951.8:n.1035-467A>G
ENST00000503472.5:n.919-467A>G
ENST00000504199.5:c.1092-467A>G	ENSP00000421725.1:n.1092-467A>G
ENST00000509740.5:c.1035-1066A>G	ENSP00000422664.1:n.1035-1066A>G
ENST00000513476.5:c.1035-467A>G	ENSP00000426683.1:n.1035-467A>G
NM_000583.3:c.1035-467A>G	NP_000574.2:n.1035-467A>G
NM_001204306.1:c.1035-467A>G	NP_001191235.1:n.1035-467A>G
NM_001204307.1:c.1092-467A>G	NP_001191236.1:n.1092-467A>G
XM_006714177.2:c.1035-467A>G	XP_006714240.1:n.1035-467A>G
XM_006714177.3:c.1035-467A>G	XP_006714240.1:n.1035-467A>G
NM_000583.4:c.1035-467A>G MANE Select	NP_000574.2:n.1035-467A>G