Canonical Allele Identifier: CA2036978772
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429855C= , CM000674.2:g.53429855C= GRCh38
NC_000012.11:g.53823639C= , CM000674.1:g.53823639C= GRCh37
NC_000012.10:g.52109906C= NCBI36
NG_015981.1:g.11001C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1165C= MANE Select ENSP00000257863.3:p.Pro389=
ENST00000257863.8:c.1165C= ENSP00000257863.3:p.Pro389=
ENST00000379791.7:c.1140+230C= ENSP00000369117.3:n.1140+230C=
ENST00000550311.5:c.1165C= ENSP00000446661.1:p.Pro389=
ENST00000550839.1:c.256C= ENSP00000455338.1:p.Pro86=
ENST00000552233.5:n.753C=
NM_001164690.1:c.1165C= NP_001158162.1:p.Pro389=
NM_001164691.1:c.1140+230C= NP_001158163.1:n.1140+230C=
NM_020547.2:c.1165C= NP_065434.1:p.Pro389=
XM_011538173.1:c.1225C= XP_011536475.1:p.Pro409=
XM_011538174.1:c.1222C= XP_011536476.1:p.Pro408=
XM_011538175.1:c.1207C= XP_011536477.1:p.Pro403=
XM_011538176.1:c.1168C= XP_011536478.1:p.Pro390=
XM_011538177.1:c.1147C= XP_011536479.1:p.Pro383=
XM_011538178.1:c.1006C= XP_011536480.1:p.Pro336=
XM_011538179.1:c.1200+230C= XP_011536481.1:n.1200+230C=
XM_011538180.1:c.892C= XP_011536482.1:p.Pro298=
XM_011538181.1:c.889C= XP_011536483.1:p.Pro297=
XM_011538182.1:c.814C= XP_011536484.1:p.Pro272=
XM_011538183.1:c.1200+230C= XP_011536485.1:n.1200+230C=
XM_011538184.1:c.1220+210C= XP_011536486.1:n.1220+210C=
XM_011538185.1:c.856-1322C= XP_011536487.1:n.856-1322C=
XM_011538186.1:c.340C= XP_011536488.1:p.Pro114=
NM_001164690.2:c.1165C= NP_001158162.1:p.Pro389=
NM_001164691.2:c.1140+230C= NP_001158163.1:n.1140+230C=
NM_020547.3:c.1165C= MANE Select NP_065434.1:p.Pro389=
XM_011538183.2:c.1200+230C= XP_011536485.1:n.1200+230C=
XM_011538184.2:c.1220+210C= XP_011536486.1:n.1220+210C=
XM_011538186.3:c.340C= XP_011536488.1:p.Pro114=
XM_017019179.2:c.1225C= XP_016874668.1:p.Pro409=
XM_024448938.1:c.1143+230C= XP_024304706.1:n.1143+230C=
XR_002957309.1:n.1133C=
XR_002957310.1:n.1108+230C=
XR_002957311.1:n.1133C=
XR_002957312.1:n.1108+230C=