Canonical Allele Identifier: CA357199297

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72607581C>T (hg19) ; chr4:g.71741864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741864C>T , CM000666.2:g.71741864C>T	GRCh38
NC_000004.11:g.72607581C>T , CM000666.1:g.72607581C>T	GRCh37
NC_000004.10:g.72826445C>T	NCBI36
NG_012837.2:g.68657G>A
NG_012837.3:g.68657G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*32G>A MANE Select	ENSP00000273951.8:n.*32G>A
ENST00000273951.12:c.*32G>A	ENSP00000273951.8:n.*32G>A
ENST00000503364.5:n.130G>A
ENST00000503472.5:n.1341G>A
ENST00000504199.5:c.*32G>A	ENSP00000421725.1:n.*32G>A
ENST00000509740.5:c.*280G>A	ENSP00000422664.1:n.*280G>A
ENST00000513476.5:c.1402G>A	ENSP00000426683.1:p.Val468Ile
NM_000583.3:c.*32G>A	NP_000574.2:n.*32G>A
NM_001204306.1:c.*32G>A	NP_001191235.1:n.*32G>A
NM_001204307.1:c.*32G>A	NP_001191236.1:n.*32G>A
XM_006714177.2:c.*46G>A	XP_006714240.1:n.*46G>A
XM_006714177.3:c.*46G>A	XP_006714240.1:n.*46G>A
NM_000583.4:c.*32G>A MANE Select	NP_000574.2:n.*32G>A