Canonical Allele Identifier: CA2318204686
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs2025057860
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251984dup , CM000681.2:g.2251984dup GRCh38
NC_000019.9:g.2251983dup , CM000681.1:g.2251983dup GRCh37
NC_000019.8:g.2202983dup NCBI36
NG_012190.1:g.7871dup
NG_032853.1:g.9443dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*27dup MANE Select ENSP00000221496.2:n.*27dup
ENST00000221496.4:c.*27dup ENSP00000221496.2:n.*27dup
NM_000479.3:c.*27dup NP_000470.2:n.*27dup
NM_000479.4:c.*27dup NP_000470.2:n.*27dup
NM_000479.5:c.*27dup MANE Select NP_000470.3:n.*27dup
Search 100 bp 5'
Search 100 bp 3'