Canonical Allele Identifier: CA1467386005
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784909C= , CM000666.2:g.71784909C= GRCh38
NC_000004.11:g.72650626C= , CM000666.1:g.72650626C= GRCh37
NC_000004.10:g.72869490C= NCBI36
NG_012837.2:g.25612G=
NG_012837.3:g.25612G=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-855G= ENSP00000421725.1:n.22-855G=
ENST00000506245.1:c.-36-855G= ENSP00000426718.1:n.-36-855G=
NM_001204306.1:c.-36-855G= NP_001191235.1:n.-36-855G=
NM_001204307.1:c.22-855G= NP_001191236.1:n.22-855G=