Canonical Allele Identifier: CA2036978786
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429879G= , CM000674.2:g.53429879G= GRCh38
NC_000012.11:g.53823663G= , CM000674.1:g.53823663G= GRCh37
NC_000012.10:g.52109930G= NCBI36
NG_015981.1:g.11025G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1189G= MANE Select ENSP00000257863.3:p.Asp397=
ENST00000257863.8:c.1189G= ENSP00000257863.3:p.Asp397=
ENST00000379791.7:c.1140+254G= ENSP00000369117.3:n.1140+254G=
ENST00000550311.5:c.1189G= ENSP00000446661.1:p.Asp397=
ENST00000550839.1:c.280G= ENSP00000455338.1:p.Asp94=
ENST00000552233.5:n.777G=
NM_001164690.1:c.1189G= NP_001158162.1:p.Asp397=
NM_001164691.1:c.1140+254G= NP_001158163.1:n.1140+254G=
NM_020547.2:c.1189G= NP_065434.1:p.Asp397=
XM_011538173.1:c.1249G= XP_011536475.1:p.Asp417=
XM_011538174.1:c.1246G= XP_011536476.1:p.Asp416=
XM_011538175.1:c.1231G= XP_011536477.1:p.Asp411=
XM_011538176.1:c.1192G= XP_011536478.1:p.Asp398=
XM_011538177.1:c.1171G= XP_011536479.1:p.Asp391=
XM_011538178.1:c.1030G= XP_011536480.1:p.Asp344=
XM_011538179.1:c.1200+254G= XP_011536481.1:n.1200+254G=
XM_011538180.1:c.916G= XP_011536482.1:p.Asp306=
XM_011538181.1:c.913G= XP_011536483.1:p.Asp305=
XM_011538182.1:c.838G= XP_011536484.1:p.Asp280=
XM_011538183.1:c.1200+254G= XP_011536485.1:n.1200+254G=
XM_011538184.1:c.1220+234G= XP_011536486.1:n.1220+234G=
XM_011538185.1:c.856-1298G= XP_011536487.1:n.856-1298G=
XM_011538186.1:c.364G= XP_011536488.1:p.Asp122=
NM_001164690.2:c.1189G= NP_001158162.1:p.Asp397=
NM_001164691.2:c.1140+254G= NP_001158163.1:n.1140+254G=
NM_020547.3:c.1189G= MANE Select NP_065434.1:p.Asp397=
XM_011538183.2:c.1200+254G= XP_011536485.1:n.1200+254G=
XM_011538184.2:c.1220+234G= XP_011536486.1:n.1220+234G=
XM_011538186.3:c.364G= XP_011536488.1:p.Asp122=
XM_017019179.2:c.1249G= XP_016874668.1:p.Asp417=
XM_024448938.1:c.1143+254G= XP_024304706.1:n.1143+254G=
XR_002957309.1:n.1157G=
XR_002957310.1:n.1108+254G=
XR_002957311.1:n.1157G=
XR_002957312.1:n.1108+254G=