Canonical Allele Identifier: CA1467351291
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1741348442
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71745906T>C , CM000666.2:g.71745906T>C GRCh38
NC_000004.11:g.72611623T>C , CM000666.1:g.72611623T>C GRCh37
NC_000004.10:g.72830487T>C NCBI36
NG_012837.2:g.64615A>G
NG_012837.3:g.64615A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*25+245A>G MANE Select ENSP00000273951.8:n.*25+245A>G
ENST00000273951.12:c.*25+245A>G ENSP00000273951.8:n.*25+245A>G
ENST00000503364.5:n.123+245A>G
ENST00000503472.5:n.1334+245A>G
ENST00000504199.5:c.*25+245A>G ENSP00000421725.1:n.*25+245A>G
ENST00000509740.5:c.*273+245A>G ENSP00000422664.1:n.*273+245A>G
ENST00000513476.5:c.1396-4036A>G ENSP00000426683.1:n.1396-4036A>G
NM_000583.3:c.*25+245A>G NP_000574.2:n.*25+245A>G
NM_001204306.1:c.*25+245A>G NP_001191235.1:n.*25+245A>G
NM_001204307.1:c.*25+245A>G NP_001191236.1:n.*25+245A>G
XM_006714177.2:c.*39+245A>G XP_006714240.1:n.*39+245A>G
XM_006714177.3:c.*39+245A>G XP_006714240.1:n.*39+245A>G
NM_000583.4:c.*25+245A>G MANE Select NP_000574.2:n.*25+245A>G
Search 100 bp 5'
Search 100 bp 3'