Canonical Allele Identifier: CA403243129
Gene: AMH HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.2251721A>C (hg19) chr19:g.2251722A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251722A>C , CM000681.2:g.2251722A>C GRCh38
NC_000019.9:g.2251721A>C , CM000681.1:g.2251721A>C GRCh37
NC_000019.8:g.2202721A>C NCBI36
NG_012190.1:g.7609A>C
NG_032853.1:g.9702T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1448A>C MANE Select ENSP00000221496.2:p.Tyr483Ser
ENST00000221496.4:c.1448A>C ENSP00000221496.2:p.Tyr483Ser
NM_000479.3:c.1448A>C NP_000470.2:p.Tyr483Ser
NM_000479.4:c.1448A>C NP_000470.2:p.Tyr483Ser
NM_000479.5:c.1448A>C MANE Select NP_000470.3:p.Tyr483Ser
Search 100 bp 5'
Search 100 bp 3'