Canonical Allele Identifier: CA2813287894

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251961del , CM000681.2:g.2251961del	GRCh38
NC_000019.9:g.2251960del , CM000681.1:g.2251960del	GRCh37
NC_000019.8:g.2202960del	NCBI36
NG_012190.1:g.7848del
NG_032853.1:g.9466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.*4del MANE Select	ENSP00000221496.2:n.*4del
ENST00000221496.4:c.*4del	ENSP00000221496.2:n.*4del
NM_000479.3:c.*4del	NP_000470.2:n.*4del
NM_000479.4:c.*4del	NP_000470.2:n.*4del
NM_000479.5:c.*4del MANE Select	NP_000470.3:n.*4del