Canonical Allele Identifier: CA2318204616
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251892T= , CM000681.2:g.2251892T= GRCh38
NC_000019.9:g.2251891T= , CM000681.1:g.2251891T= GRCh37
NC_000019.8:g.2202891T= NCBI36
NG_012190.1:g.7779T=
NG_032853.1:g.9532A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1618T= MANE Select ENSP00000221496.2:p.Ser540=
ENST00000221496.4:c.1618T= ENSP00000221496.2:p.Ser540=
NM_000479.3:c.1618T= NP_000470.2:p.Ser540=
NM_000479.4:c.1618T= NP_000470.2:p.Ser540=
NM_000479.5:c.1618T= MANE Select NP_000470.3:p.Ser540=