Canonical Allele Identifier: CA99061189

Gene: GC

Linked Data

• dbSNP Id: rs1029817081
• MyVariant Identifiers: chr4:g.72614349G>A (hg19) ; chr4:g.71748632G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71748632G>A , CM000666.2:g.71748632G>A	GRCh38
NC_000004.11:g.72614349G>A , CM000666.1:g.72614349G>A	GRCh37
NC_000004.10:g.72833213G>A	NCBI36
NG_012837.2:g.61889C>T
NG_012837.3:g.61889C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1396-2427C>T MANE Select	ENSP00000273951.8:n.1396-2427C>T
ENST00000273951.12:c.1396-2427C>T	ENSP00000273951.8:n.1396-2427C>T
ENST00000503364.5:n.69-2427C>T
ENST00000503472.5:n.1280-2427C>T
ENST00000504199.5:c.1453-2427C>T	ENSP00000421725.1:n.1453-2427C>T
ENST00000509740.5:c.*219-2427C>T	ENSP00000422664.1:n.*219-2427C>T
ENST00000513476.5:c.1395+3886C>T	ENSP00000426683.1:n.1395+3886C>T
NM_000583.3:c.1396-2427C>T	NP_000574.2:n.1396-2427C>T
NM_001204306.1:c.1396-2427C>T	NP_001191235.1:n.1396-2427C>T
NM_001204307.1:c.1453-2427C>T	NP_001191236.1:n.1453-2427C>T
XM_006714177.2:c.1263-2427C>T	XP_006714240.1:n.1263-2427C>T
XM_006714177.3:c.1263-2427C>T	XP_006714240.1:n.1263-2427C>T
NM_000583.4:c.1396-2427C>T MANE Select	NP_000574.2:n.1396-2427C>T