Canonical Allele Identifier: CA403243785

Gene: AMH

Linked Data

• MyVariant Identifiers: chr19:g.2251924A>C (hg19) ; chr19:g.2251925A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251925A>C , CM000681.2:g.2251925A>C	GRCh38
NC_000019.9:g.2251924A>C , CM000681.1:g.2251924A>C	GRCh37
NC_000019.8:g.2202924A>C	NCBI36
NG_012190.1:g.7812A>C
NG_032853.1:g.9499T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.1651A>C MANE Select	ENSP00000221496.2:p.Asn551His
ENST00000221496.4:c.1651A>C	ENSP00000221496.2:p.Asn551His
NM_000479.3:c.1651A>C	NP_000470.2:p.Asn551His
NM_000479.4:c.1651A>C	NP_000470.2:p.Asn551His
NM_000479.5:c.1651A>C MANE Select	NP_000470.3:p.Asn551His