Canonical Allele Identifier: CA403243098
Gene: AMH HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.2251706T>A (hg19) chr19:g.2251707T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251707T>A , CM000681.2:g.2251707T>A GRCh38
NC_000019.9:g.2251706T>A , CM000681.1:g.2251706T>A GRCh37
NC_000019.8:g.2202706T>A NCBI36
NG_012190.1:g.7594T>A
NG_032853.1:g.9717A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1433T>A MANE Select ENSP00000221496.2:p.Leu478His
ENST00000221496.4:c.1433T>A ENSP00000221496.2:p.Leu478His
NM_000479.3:c.1433T>A NP_000470.2:p.Leu478His
NM_000479.4:c.1433T>A NP_000470.2:p.Leu478His
NM_000479.5:c.1433T>A MANE Select NP_000470.3:p.Leu478His
Search 100 bp 5'
Search 100 bp 3'