Canonical Allele Identifier: CA2583853144
Gene: AMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251415del , CM000681.2:g.2251415del GRCh38
NC_000019.9:g.2251414del , CM000681.1:g.2251414del GRCh37
NC_000019.8:g.2202414del NCBI36
NG_012190.1:g.7302del
NG_032853.1:g.10009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1141del MANE Select ENSP00000221496.2:p.Ala381LeufsTer?
ENST00000221496.4:c.1141del ENSP00000221496.2:p.Ala381LeufsTer?
ENST00000589313.2:n.1494del
NM_000479.3:c.1141del NP_000470.2:p.Ala381LeufsTer?
NM_000479.4:c.1141del NP_000470.2:p.Ala381LeufsTer?
NM_000479.5:c.1141del MANE Select NP_000470.3:p.Ala381LeufsTer?