Canonical Allele Identifier: CA99057588

Gene: GC

Linked Data

• dbSNP Id: rs1022761146
• gnomAD v3: 4-71742351-C-A
• gnomAD v4: 4-71742351-C-A
• MyVariant Identifiers: chr4:g.72608068C>A (hg19) ; chr4:g.71742351C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742351C>A , CM000666.2:g.71742351C>A	GRCh38
NC_000004.11:g.72608068C>A , CM000666.1:g.72608068C>A	GRCh37
NC_000004.10:g.72826932C>A	NCBI36
NG_012837.2:g.68170G>T
NG_012837.3:g.68170G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*26-481G>T MANE Select	ENSP00000273951.8:n.*26-481G>T
ENST00000273951.12:c.*26-481G>T	ENSP00000273951.8:n.*26-481G>T
ENST00000503364.5:n.124-481G>T
ENST00000503472.5:n.1335-481G>T
ENST00000504199.5:c.*26-481G>T	ENSP00000421725.1:n.*26-481G>T
ENST00000509740.5:c.*274-481G>T	ENSP00000422664.1:n.*274-481G>T
ENST00000513476.5:c.1396-481G>T	ENSP00000426683.1:n.1396-481G>T
NM_000583.3:c.*26-481G>T	NP_000574.2:n.*26-481G>T
NM_001204306.1:c.*26-481G>T	NP_001191235.1:n.*26-481G>T
NM_001204307.1:c.*26-481G>T	NP_001191236.1:n.*26-481G>T
XM_006714177.2:c.*40-481G>T	XP_006714240.1:n.*40-481G>T
XM_006714177.3:c.*40-481G>T	XP_006714240.1:n.*40-481G>T
NM_000583.4:c.*26-481G>T MANE Select	NP_000574.2:n.*26-481G>T