Canonical Allele Identifier: CA2583853235
Gene: AMH HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000019.10:g.2251986A>G , CM000681.2:g.2251986A>G GRCh38
NC_000019.9:g.2251985A>G , CM000681.1:g.2251985A>G GRCh37
NC_000019.8:g.2202985A>G NCBI36
NG_012190.1:g.7873A>G
NG_032853.1:g.9438T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*29A>G MANE Select ENSP00000221496.2:n.*29A>G
ENST00000221496.4:c.*29A>G ENSP00000221496.2:n.*29A>G
NM_000479.3:c.*29A>G NP_000470.2:n.*29A>G
NM_000479.4:c.*29A>G NP_000470.2:n.*29A>G
NM_000479.5:c.*29A>G MANE Select NP_000470.3:n.*29A>G
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Search 100 bp 3'