Canonical Allele Identifier: CA403243319
Gene: AMH HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.2251780T>A (hg19) chr19:g.2251781T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251781T>A , CM000681.2:g.2251781T>A GRCh38
NC_000019.9:g.2251780T>A , CM000681.1:g.2251780T>A GRCh37
NC_000019.8:g.2202780T>A NCBI36
NG_012190.1:g.7668T>A
NG_032853.1:g.9643A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1507T>A MANE Select ENSP00000221496.2:p.Tyr503Asn
ENST00000221496.4:c.1507T>A ENSP00000221496.2:p.Tyr503Asn
NM_000479.3:c.1507T>A NP_000470.2:p.Tyr503Asn
NM_000479.4:c.1507T>A NP_000470.2:p.Tyr503Asn
NM_000479.5:c.1507T>A MANE Select NP_000470.3:p.Tyr503Asn
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