Canonical Allele Identifier: CA2583853143
Gene: AMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251407_2251493del , CM000681.2:g.2251407_2251493del GRCh38
NC_000019.9:g.2251406_2251492del , CM000681.1:g.2251406_2251492del GRCh37
NC_000019.8:g.2202406_2202492del NCBI36
NG_012190.1:g.7294_7380del
NG_032853.1:g.9941_10027del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1133_1219del MANE Select ENSP00000221496.2:p.Arg378_Arg406del
ENST00000221496.4:c.1133_1219del ENSP00000221496.2:p.Arg378_Arg406del
ENST00000589313.2:n.1486_1572del
NM_000479.3:c.1133_1219del NP_000470.2:p.Arg378_Arg406del
NM_000479.4:c.1133_1219del NP_000470.2:p.Arg378_Arg406del
NM_000479.5:c.1133_1219del MANE Select NP_000470.3:p.Arg378_Arg406del