Canonical Allele Identifier: CA2318204406
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251547C= , CM000681.2:g.2251547C= GRCh38
NC_000019.9:g.2251546C= , CM000681.1:g.2251546C= GRCh37
NC_000019.8:g.2202546C= NCBI36
NG_012190.1:g.7434C=
NG_032853.1:g.9877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1273C= MANE Select ENSP00000221496.2:p.Leu425=
ENST00000221496.4:c.1273C= ENSP00000221496.2:p.Leu425=
ENST00000589313.2:n.1626C=
NM_000479.3:c.1273C= NP_000470.2:p.Leu425=
NM_000479.4:c.1273C= NP_000470.2:p.Leu425=
NM_000479.5:c.1273C= MANE Select NP_000470.3:p.Leu425=