Canonical Allele Identifier: CA759848325
Gene: GCG HGNC NCBI

Linked Data

dbSNP Id: rs183433761
gnomAD v3: 2-162152278-T-G
gnomAD v4: 2-162152278-T-G
MyVariant Identifiers: chr2:g.163008788T>G (hg19) chr2:g.162152278T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162152278T>G , CM000664.2:g.162152278T>G GRCh38
NC_000002.11:g.163008788T>G , CM000664.1:g.163008788T>G GRCh37
NC_000002.10:g.162717034T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375497.3:c.-130A>C ENSP00000364647.3:n.-130A>C
ENST00000418842.6:c.-130A>C ENSP00000387662.2:n.-130A>C
NM_002054.4:c.-130A>C NP_002045.1:n.-130A>C
NR_110255.1:n.93-9492T>G
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