Canonical Allele Identifier: CA2583853236
Gene: AMH HGNC NCBI

Linked Data

gnomAD v4: 19-2251986-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251989del , CM000681.2:g.2251989del GRCh38
NC_000019.9:g.2251988del , CM000681.1:g.2251988del GRCh37
NC_000019.8:g.2202988del NCBI36
NG_012190.1:g.7876del
NG_032853.1:g.9437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*32del MANE Select ENSP00000221496.2:n.*32del
ENST00000221496.4:c.*32del ENSP00000221496.2:n.*32del
NM_000479.3:c.*32del NP_000470.2:n.*32del
NM_000479.4:c.*32del NP_000470.2:n.*32del
NM_000479.5:c.*32del MANE Select NP_000470.3:n.*32del
Search 100 bp 5'
Search 100 bp 3'