Canonical Allele Identifier: CA403243816
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs2025056575
gnomAD v4: 19-2251932-T-C
MyVariant Identifiers: chr19:g.2251931T>C (hg19) chr19:g.2251932T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251932T>C , CM000681.2:g.2251932T>C GRCh38
NC_000019.9:g.2251931T>C , CM000681.1:g.2251931T>C GRCh37
NC_000019.8:g.2202931T>C NCBI36
NG_012190.1:g.7819T>C
NG_032853.1:g.9492A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1658T>C MANE Select ENSP00000221496.2:p.Val553Ala
ENST00000221496.4:c.1658T>C ENSP00000221496.2:p.Val553Ala
NM_000479.3:c.1658T>C NP_000470.2:p.Val553Ala
NM_000479.4:c.1658T>C NP_000470.2:p.Val553Ala
NM_000479.5:c.1658T>C MANE Select NP_000470.3:p.Val553Ala
Search 100 bp 5'
Search 100 bp 3'