Canonical Allele Identifier: CA2318204449
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251627C= , CM000681.2:g.2251627C= GRCh38
NC_000019.9:g.2251626C= , CM000681.1:g.2251626C= GRCh37
NC_000019.8:g.2202626C= NCBI36
NG_012190.1:g.7514C=
NG_032853.1:g.9797G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1353C= MANE Select ENSP00000221496.2:p.Arg451=
ENST00000221496.4:c.1353C= ENSP00000221496.2:p.Arg451=
NM_000479.3:c.1353C= NP_000470.2:p.Arg451=
NM_000479.4:c.1353C= NP_000470.2:p.Arg451=
NM_000479.5:c.1353C= MANE Select NP_000470.3:p.Arg451=