Canonical Allele Identifier: CA403243817
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs2025056575

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251932T>G , CM000681.2:g.2251932T>G GRCh38
NC_000019.9:g.2251931T>G , CM000681.1:g.2251931T>G GRCh37
NC_000019.8:g.2202931T>G NCBI36
NG_012190.1:g.7819T>G
NG_032853.1:g.9492A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1658T>G MANE Select ENSP00000221496.2:p.Val553Gly
ENST00000221496.4:c.1658T>G ENSP00000221496.2:p.Val553Gly
NM_000479.3:c.1658T>G NP_000470.2:p.Val553Gly
NM_000479.4:c.1658T>G NP_000470.2:p.Val553Gly
NM_000479.5:c.1658T>G MANE Select NP_000470.3:p.Val553Gly