Canonical Allele Identifier: CA1747110225
Gene: KLRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.139458699C>T , CM000669.2:g.139458699C>T GRCh38
NC_000007.13:g.139143445C>T , CM000669.1:g.139143445C>T GRCh37
NC_000007.12:g.138793985C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000340940.5:c.1006-4485G>A MANE Select ENSP00000339356.4:n.1006-4485G>A
ENST00000340940.4:c.1006-4485G>A ENSP00000339356.4:n.1006-4485G>A
ENST00000393039.2:c.758-4992G>A ENSP00000376759.2:n.758-4992G>A
NM_198508.2:c.1006-4485G>A NP_940910.1:n.1006-4485G>A
XM_005250311.2:c.1006-4992G>A XP_005250368.1:n.1006-4992G>A
XM_011516141.1:c.1005+20928G>A XP_011514443.1:n.1005+20928G>A
NM_198508.3:c.1006-4485G>A NP_940910.1:n.1006-4485G>A
XM_005250311.3:c.1006-4992G>A XP_005250368.1:n.1006-4992G>A
XM_011516141.2:c.1005+20928G>A XP_011514443.1:n.1005+20928G>A
NM_198508.4:c.1006-4485G>A MANE Select NP_940910.1:n.1006-4485G>A