Canonical Allele Identifier: CA2535090220
Gene: GCKR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27519740G>T , CM000664.2:g.27519740G>T GRCh38
NC_000002.11:g.27742607G>T , CM000664.1:g.27742607G>T GRCh37
NC_000002.10:g.27596111G>T NCBI36
NG_028024.1:g.27902G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264717.7:c.1572+803G>T MANE Select ENSP00000264717.2:n.1572+803G>T
ENST00000264717.6:c.1572+803G>T ENSP00000264717.2:n.1572+803G>T
NM_001486.3:c.1572+803G>T NP_001477.2:n.1572+803G>T
XM_011532761.1:c.1419+803G>T XP_011531063.1:n.1419+803G>T
XM_011532762.1:c.1002+803G>T XP_011531064.1:n.1002+803G>T
XM_017003796.1:c.1002+803G>T XP_016859285.1:n.1002+803G>T
XM_017003797.1:c.1002+803G>T XP_016859286.1:n.1002+803G>T
NM_001486.4:c.1572+803G>T MANE Select NP_001477.2:n.1572+803G>T
Search 100 bp 5'
Search 100 bp 3'