Canonical Allele Identifier: CA507776
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs769722871
gnomAD v2: 1-957567-C-T
gnomAD v4: 1-1022187-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1022187C>T , CM000663.2:g.1022187C>T GRCh38
NC_000001.10:g.957567C>T , CM000663.1:g.957567C>T GRCh37
NC_000001.9:g.947430C>T NCBI36
NG_016346.1:g.7065C>T , LRG_198:g.7065C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.202-14C>T MANE Select ENSP00000368678.2:n.202-14C>T
ENST00000379370.6:c.202-14C>T ENSP00000368678.2:n.202-14C>T
ENST00000620552.4:c.-213-14C>T ENSP00000484607.1:n.-213-14C>T
NM_001305275.1:c.202-14C>T NP_001292204.1:n.202-14C>T
NM_198576.3:c.202-14C>T NP_940978.2:n.202-14C>T
XM_005244749.2:c.202-14C>T XP_005244806.1:n.202-14C>T
XM_006710635.2:c.202-14C>T XP_006710698.1:n.202-14C>T
XM_011541429.1:c.202-14C>T XP_011539731.1:n.202-14C>T
XM_011541430.1:c.202-14C>T XP_011539732.1:n.202-14C>T
XR_946650.1:n.269-14C>T
XM_005244749.3:c.202-14C>T XP_005244806.1:n.202-14C>T
XM_011541429.2:c.202-14C>T XP_011539731.1:n.202-14C>T
XR_946650.2:n.273-14C>T
NM_001305275.2:c.202-14C>T NP_001292204.1:n.202-14C>T
NM_198576.4:c.202-14C>T MANE Select NP_940978.2:n.202-14C>T