Canonical Allele Identifier: CA2580589239

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71783222A>C , CM000666.2:g.71783222A>C	GRCh38
NC_000004.11:g.72648939A>C , CM000666.1:g.72648939A>C	GRCh37
NC_000004.10:g.72867803A>C	NCBI36
NG_012837.2:g.27299T>G
NG_012837.3:g.27299T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.58+739T>G MANE Select	ENSP00000273951.8:n.58+739T>G
ENST00000273951.12:c.58+739T>G	ENSP00000273951.8:n.58+739T>G
ENST00000504199.5:c.115+739T>G	ENSP00000421725.1:n.115+739T>G
ENST00000506245.1:c.58+739T>G	ENSP00000426718.1:n.58+739T>G
ENST00000509740.5:c.58+739T>G	ENSP00000422664.1:n.58+739T>G
ENST00000513476.5:c.58+739T>G	ENSP00000426683.1:n.58+739T>G
NM_000583.3:c.58+739T>G	NP_000574.2:n.58+739T>G
NM_001204306.1:c.58+739T>G	NP_001191235.1:n.58+739T>G
NM_001204307.1:c.115+739T>G	NP_001191236.1:n.115+739T>G
XM_006714177.2:c.58+739T>G	XP_006714240.1:n.58+739T>G
XM_006714177.3:c.58+739T>G	XP_006714240.1:n.58+739T>G
NM_000583.4:c.58+739T>G MANE Select	NP_000574.2:n.58+739T>G