Canonical Allele Identifier: CA1747110224
Gene: KLRG2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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