Canonical Allele Identifier: CA505143690
Gene: AMH HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.2251728C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251729C>A , CM000681.2:g.2251729C>A GRCh38
NC_000019.9:g.2251728C>A , CM000681.1:g.2251728C>A GRCh37
NC_000019.8:g.2202728C>A NCBI36
NG_012190.1:g.7616C>A
NG_032853.1:g.9695G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221496.5:c.1455C>A MANE Select ENSP00000221496.2:p.Ala485=
ENST00000221496.4:c.1455C>A ENSP00000221496.2:p.Ala485=
NM_000479.3:c.1455C>A NP_000470.2:p.Ala485=
NM_000479.4:c.1455C>A NP_000470.2:p.Ala485=
NM_000479.5:c.1455C>A MANE Select NP_000470.3:p.Ala485=
Search 100 bp 5'
Search 100 bp 3'