Canonical Allele Identifier: CA2036978779
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429871A= , CM000674.2:g.53429871A= GRCh38
NC_000012.11:g.53823655A= , CM000674.1:g.53823655A= GRCh37
NC_000012.10:g.52109922A= NCBI36
NG_015981.1:g.11017A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1181A= MANE Select ENSP00000257863.3:p.Lys394=
ENST00000257863.8:c.1181A= ENSP00000257863.3:p.Lys394=
ENST00000379791.7:c.1140+246A= ENSP00000369117.3:n.1140+246A=
ENST00000550311.5:c.1181A= ENSP00000446661.1:p.Lys394=
ENST00000550839.1:c.272A= ENSP00000455338.1:p.Lys91=
ENST00000552233.5:n.769A=
NM_001164690.1:c.1181A= NP_001158162.1:p.Lys394=
NM_001164691.1:c.1140+246A= NP_001158163.1:n.1140+246A=
NM_020547.2:c.1181A= NP_065434.1:p.Lys394=
XM_011538173.1:c.1241A= XP_011536475.1:p.Lys414=
XM_011538174.1:c.1238A= XP_011536476.1:p.Lys413=
XM_011538175.1:c.1223A= XP_011536477.1:p.Lys408=
XM_011538176.1:c.1184A= XP_011536478.1:p.Lys395=
XM_011538177.1:c.1163A= XP_011536479.1:p.Lys388=
XM_011538178.1:c.1022A= XP_011536480.1:p.Lys341=
XM_011538179.1:c.1200+246A= XP_011536481.1:n.1200+246A=
XM_011538180.1:c.908A= XP_011536482.1:p.Lys303=
XM_011538181.1:c.905A= XP_011536483.1:p.Lys302=
XM_011538182.1:c.830A= XP_011536484.1:p.Lys277=
XM_011538183.1:c.1200+246A= XP_011536485.1:n.1200+246A=
XM_011538184.1:c.1220+226A= XP_011536486.1:n.1220+226A=
XM_011538185.1:c.856-1306A= XP_011536487.1:n.856-1306A=
XM_011538186.1:c.356A= XP_011536488.1:p.Lys119=
NM_001164690.2:c.1181A= NP_001158162.1:p.Lys394=
NM_001164691.2:c.1140+246A= NP_001158163.1:n.1140+246A=
NM_020547.3:c.1181A= MANE Select NP_065434.1:p.Lys394=
XM_011538183.2:c.1200+246A= XP_011536485.1:n.1200+246A=
XM_011538184.2:c.1220+226A= XP_011536486.1:n.1220+226A=
XM_011538186.3:c.356A= XP_011536488.1:p.Lys119=
XM_017019179.2:c.1241A= XP_016874668.1:p.Lys414=
XM_024448938.1:c.1143+246A= XP_024304706.1:n.1143+246A=
XR_002957309.1:n.1149A=
XR_002957310.1:n.1108+246A=
XR_002957311.1:n.1149A=
XR_002957312.1:n.1108+246A=