Canonical Allele Identifier: CA403242656
Gene: AMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251560A>C , CM000681.2:g.2251560A>C GRCh38
NC_000019.9:g.2251559A>C , CM000681.1:g.2251559A>C GRCh37
NC_000019.8:g.2202559A>C NCBI36
NG_012190.1:g.7447A>C
NG_032853.1:g.9864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1286A>C MANE Select ENSP00000221496.2:p.Lys429Thr
ENST00000221496.4:c.1286A>C ENSP00000221496.2:p.Lys429Thr
ENST00000589313.2:n.1639A>C
NM_000479.3:c.1286A>C NP_000470.2:p.Lys429Thr
NM_000479.4:c.1286A>C NP_000470.2:p.Lys429Thr
NM_000479.5:c.1286A>C MANE Select NP_000470.3:p.Lys429Thr