Canonical Allele Identifier: CA505143069
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs780065671
gnomAD v3: 19-2251903-C-T
gnomAD v4: 19-2251903-C-T
MyVariant Identifiers: chr19:g.2251902C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251903C>T , CM000681.2:g.2251903C>T GRCh38
NC_000019.9:g.2251902C>T , CM000681.1:g.2251902C>T GRCh37
NC_000019.8:g.2202902C>T NCBI36
NG_012190.1:g.7790C>T
NG_032853.1:g.9521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1629C>T MANE Select ENSP00000221496.2:p.Arg543=
ENST00000221496.4:c.1629C>T ENSP00000221496.2:p.Arg543=
NM_000479.3:c.1629C>T NP_000470.2:p.Arg543=
NM_000479.4:c.1629C>T NP_000470.2:p.Arg543=
NM_000479.5:c.1629C>T MANE Select NP_000470.3:p.Arg543=
Search 100 bp 5'
Search 100 bp 3'