Canonical Allele Identifier: CA1467382715
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1742554019
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71777805dup , CM000666.2:g.71777805dup GRCh38
NC_000004.11:g.72643522dup , CM000666.1:g.72643522dup GRCh37
NC_000004.10:g.72862386dup NCBI36
NG_012837.2:g.32720dup
NG_012837.3:g.32720dup

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.58+6160dup MANE Select ENSP00000273951.8:n.58+6160dup
ENST00000273951.12:c.58+6160dup ENSP00000273951.8:n.58+6160dup
ENST00000504199.5:c.115+6160dup ENSP00000421725.1:n.115+6160dup
ENST00000506245.1:c.58+6160dup ENSP00000426718.1:n.58+6160dup
ENST00000509740.5:c.58+6160dup ENSP00000422664.1:n.58+6160dup
ENST00000513476.5:c.58+6160dup ENSP00000426683.1:n.58+6160dup
NM_000583.3:c.58+6160dup NP_000574.2:n.58+6160dup
NM_001204306.1:c.58+6160dup NP_001191235.1:n.58+6160dup
NM_001204307.1:c.115+6160dup NP_001191236.1:n.115+6160dup
XM_006714177.2:c.58+6160dup XP_006714240.1:n.58+6160dup
XM_006714177.3:c.58+6160dup XP_006714240.1:n.58+6160dup
NM_000583.4:c.58+6160dup MANE Select NP_000574.2:n.58+6160dup
Search 100 bp 5'
Search 100 bp 3'