Canonical Allele Identifier: CA9063150
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs780333296
ExAC: 19:2251990 C / G
gnomAD v2: 19-2251990-C-G
gnomAD v3: 19-2251991-C-G
gnomAD v4: 19-2251991-C-G
MyVariant Identifiers: chr19:g.2251990C>G (hg19) chr19:g.2251991C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251991C>G , CM000681.2:g.2251991C>G GRCh38
NC_000019.9:g.2251990C>G , CM000681.1:g.2251990C>G GRCh37
NC_000019.8:g.2202990C>G NCBI36
NG_012190.1:g.7878C>G
NG_032853.1:g.9433G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*34C>G MANE Select ENSP00000221496.2:n.*34C>G
ENST00000221496.4:c.*34C>G ENSP00000221496.2:n.*34C>G
NM_000479.3:c.*34C>G NP_000470.2:n.*34C>G
NM_000479.4:c.*34C>G NP_000470.2:n.*34C>G
NM_000479.5:c.*34C>G MANE Select NP_000470.3:n.*34C>G
Search 100 bp 5'
Search 100 bp 3'