Canonical Allele Identifier: CA439799485

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72649748G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784031G>T , CM000666.2:g.71784031G>T	GRCh38
NC_000004.11:g.72649748G>T , CM000666.1:g.72649748G>T	GRCh37
NC_000004.10:g.72868612G>T	NCBI36
NG_012837.2:g.26490C>A
NG_012837.3:g.26490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.-13C>A MANE Select	ENSP00000273951.8:n.-13C>A
ENST00000273951.12:c.-13C>A	ENSP00000273951.8:n.-13C>A
ENST00000504199.5:c.45C>A	ENSP00000421725.1:p.Leu15=
ENST00000506245.1:c.-13C>A	ENSP00000426718.1:n.-13C>A
ENST00000509740.5:c.-13C>A	ENSP00000422664.1:n.-13C>A
ENST00000513476.5:c.-13C>A	ENSP00000426683.1:n.-13C>A
NM_000583.3:c.-13C>A	NP_000574.2:n.-13C>A
NM_001204306.1:c.-13C>A	NP_001191235.1:n.-13C>A
NM_001204307.1:c.45C>A	NP_001191236.1:p.Leu15=
XM_006714177.2:c.-13C>A	XP_006714240.1:n.-13C>A
XM_006714177.3:c.-13C>A	XP_006714240.1:n.-13C>A
NM_000583.4:c.-13C>A MANE Select	NP_000574.2:n.-13C>A