Canonical Allele Identifier: CA99487280
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs985266553
MyVariant Identifiers: chr4:g.72656375G>A (hg19) chr4:g.71790658G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71790658G>A , CM000666.2:g.71790658G>A GRCh38
NC_000004.11:g.72656375G>A , CM000666.1:g.72656375G>A GRCh37
NC_000004.10:g.72875239G>A NCBI36
NG_012837.2:g.19863C>T
NG_012837.3:g.19863C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-6604C>T ENSP00000421725.1:n.22-6604C>T
NM_001204306.1:c.-36-6604C>T NP_001191235.1:n.-36-6604C>T
NM_001204307.1:c.22-6604C>T NP_001191236.1:n.22-6604C>T
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