Canonical Allele Identifier: CA2318204690
Gene: AMH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251983C= , CM000681.2:g.2251983C= GRCh38
NC_000019.9:g.2251982C= , CM000681.1:g.2251982C= GRCh37
NC_000019.8:g.2202982C= NCBI36
NG_012190.1:g.7870C=
NG_032853.1:g.9441G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*26C= MANE Select ENSP00000221496.2:n.*26C=
ENST00000221496.4:c.*26C= ENSP00000221496.2:n.*26C=
NM_000479.3:c.*26C= NP_000470.2:n.*26C=
NM_000479.4:c.*26C= NP_000470.2:n.*26C=
NM_000479.5:c.*26C= MANE Select NP_000470.3:n.*26C=
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