Canonical Allele Identifier: CA2515168873
Gene: AMH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251973G>C , CM000681.2:g.2251973G>C GRCh38
NC_000019.9:g.2251972G>C , CM000681.1:g.2251972G>C GRCh37
NC_000019.8:g.2202972G>C NCBI36
NG_012190.1:g.7860G>C
NG_032853.1:g.9451C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*16G>C MANE Select ENSP00000221496.2:n.*16G>C
ENST00000221496.4:c.*16G>C ENSP00000221496.2:n.*16G>C
NM_000479.3:c.*16G>C NP_000470.2:n.*16G>C
NM_000479.4:c.*16G>C NP_000470.2:n.*16G>C
NM_000479.5:c.*16G>C MANE Select NP_000470.3:n.*16G>C
Search 100 bp 5'
Search 100 bp 3'