Canonical Allele Identifier: CA2318204672
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251967C= , CM000681.2:g.2251967C= GRCh38
NC_000019.9:g.2251966C= , CM000681.1:g.2251966C= GRCh37
NC_000019.8:g.2202966C= NCBI36
NG_012190.1:g.7854C=
NG_032853.1:g.9457G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*10C= MANE Select ENSP00000221496.2:n.*10C=
ENST00000221496.4:c.*10C= ENSP00000221496.2:n.*10C=
NM_000479.3:c.*10C= NP_000470.2:n.*10C=
NM_000479.4:c.*10C= NP_000470.2:n.*10C=
NM_000479.5:c.*10C= MANE Select NP_000470.3:n.*10C=