Canonical Allele Identifier: CA2015347147

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116207G= , CM000674.2:g.9116207G= GRCh38
NC_000012.11:g.9268803G= , CM000674.1:g.9268803G= GRCh37
NC_000012.10:g.9160070G= NCBI36
NG_011717.1:g.4756C=
NG_011717.2:g.4756C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-97C= (A2M) ENSP00000385710.2:n.-97C=
NM_000014.5:c.-358C= (A2M) NP_000005.2:n.-358C=
NM_001347423.1:c.-97C= (A2M) NP_001334352.1:n.-97C=
NM_001347424.1:c.-811C= (A2M) NP_001334353.1:n.-811C=
NM_001347425.1:c.-648C= (A2M) NP_001334354.1:n.-648C=
XM_017018683.1:c.*34-9167G= (KLRG1) XP_016874172.1:n.*34-9167G=
XM_017018684.1:c.*34-18879G= (KLRG1) XP_016874173.1:n.*34-18879G=
XM_017018685.1:c.*33+58041G= (KLRG1) XP_016874174.1:n.*33+58041G=
NM_001347423.2:c.-97C= (A2M) NP_001334352.2:n.-97C=