Canonical Allele Identifier: CA99074761
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs555474392
gnomAD v3: 4-71784788-A-T
gnomAD v4: 4-71784788-A-T
MyVariant Identifiers: chr4:g.72650505A>T (hg19) chr4:g.71784788A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784788A>T , CM000666.2:g.71784788A>T GRCh38
NC_000004.11:g.72650505A>T , CM000666.1:g.72650505A>T GRCh37
NC_000004.10:g.72869369A>T NCBI36
NG_012837.2:g.25733T>A
NG_012837.3:g.25733T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-734T>A ENSP00000421725.1:n.22-734T>A
ENST00000506245.1:c.-36-734T>A ENSP00000426718.1:n.-36-734T>A
NM_001204306.1:c.-36-734T>A NP_001191235.1:n.-36-734T>A
NM_001204307.1:c.22-734T>A NP_001191236.1:n.22-734T>A
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