Canonical Allele Identifier: CA631305924
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs1568395304

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251932_2251934del , CM000681.2:g.2251932_2251934del GRCh38
NC_000019.9:g.2251931_2251933del , CM000681.1:g.2251931_2251933del GRCh37
NC_000019.8:g.2202931_2202933del NCBI36
NG_012190.1:g.7819_7821del
NG_032853.1:g.9493_9495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1658_1660del MANE Select ENSP00000221496.2:p.Val553del
ENST00000221496.4:c.1658_1660del ENSP00000221496.2:p.Val553del
NM_000479.3:c.1658_1660del NP_000470.2:p.Val553del
NM_000479.4:c.1658_1660del NP_000470.2:p.Val553del
NM_000479.5:c.1658_1660del MANE Select NP_000470.3:p.Val553del