Canonical Allele Identifier: CA403243833

Gene: AMH

Linked Data

• gnomAD v4: 19-2251938-C-A
• MyVariant Identifiers: chr19:g.2251937C>A (hg19) ; chr19:g.2251938C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251938C>A , CM000681.2:g.2251938C>A	GRCh38
NC_000019.9:g.2251937C>A , CM000681.1:g.2251937C>A	GRCh37
NC_000019.8:g.2202937C>A	NCBI36
NG_012190.1:g.7825C>A
NG_032853.1:g.9486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.1664C>A MANE Select	ENSP00000221496.2:p.Thr555Asn
ENST00000221496.4:c.1664C>A	ENSP00000221496.2:p.Thr555Asn
NM_000479.3:c.1664C>A	NP_000470.2:p.Thr555Asn
NM_000479.4:c.1664C>A	NP_000470.2:p.Thr555Asn
NM_000479.5:c.1664C>A MANE Select	NP_000470.3:p.Thr555Asn