Canonical Allele Identifier: CA767408141
Gene: GCKR HGNC NCBI

Linked Data

dbSNP Id: rs1469519920
MyVariant Identifiers: chr2:g.27742665G>C (hg19) chr2:g.27519798G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27519798G>C , CM000664.2:g.27519798G>C GRCh38
NC_000002.11:g.27742665G>C , CM000664.1:g.27742665G>C GRCh37
NC_000002.10:g.27596169G>C NCBI36
NG_028024.1:g.27960G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264717.7:c.1572+861G>C MANE Select ENSP00000264717.2:n.1572+861G>C
ENST00000264717.6:c.1572+861G>C ENSP00000264717.2:n.1572+861G>C
NM_001486.3:c.1572+861G>C NP_001477.2:n.1572+861G>C
XM_011532761.1:c.1419+861G>C XP_011531063.1:n.1419+861G>C
XM_011532762.1:c.1002+861G>C XP_011531064.1:n.1002+861G>C
XM_017003796.1:c.1002+861G>C XP_016859285.1:n.1002+861G>C
XM_017003797.1:c.1002+861G>C XP_016859286.1:n.1002+861G>C
NM_001486.4:c.1572+861G>C MANE Select NP_001477.2:n.1572+861G>C
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