Canonical Allele Identifier: CA2036978766
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429851G= , CM000674.2:g.53429851G= GRCh38
NC_000012.11:g.53823635G= , CM000674.1:g.53823635G= GRCh37
NC_000012.10:g.52109902G= NCBI36
NG_015981.1:g.10997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1161G= MANE Select ENSP00000257863.3:p.Met387=
ENST00000257863.8:c.1161G= ENSP00000257863.3:p.Met387=
ENST00000379791.7:c.1140+226G= ENSP00000369117.3:n.1140+226G=
ENST00000550311.5:c.1161G= ENSP00000446661.1:p.Met387=
ENST00000550839.1:c.252G= ENSP00000455338.1:p.Met84=
ENST00000552233.5:n.749G=
NM_001164690.1:c.1161G= NP_001158162.1:p.Met387=
NM_001164691.1:c.1140+226G= NP_001158163.1:n.1140+226G=
NM_020547.2:c.1161G= NP_065434.1:p.Met387=
XM_011538173.1:c.1221G= XP_011536475.1:p.Met407=
XM_011538174.1:c.1218G= XP_011536476.1:p.Met406=
XM_011538175.1:c.1203G= XP_011536477.1:p.Met401=
XM_011538176.1:c.1164G= XP_011536478.1:p.Met388=
XM_011538177.1:c.1143G= XP_011536479.1:p.Met381=
XM_011538178.1:c.1002G= XP_011536480.1:p.Met334=
XM_011538179.1:c.1200+226G= XP_011536481.1:n.1200+226G=
XM_011538180.1:c.888G= XP_011536482.1:p.Met296=
XM_011538181.1:c.885G= XP_011536483.1:p.Met295=
XM_011538182.1:c.810G= XP_011536484.1:p.Met270=
XM_011538183.1:c.1200+226G= XP_011536485.1:n.1200+226G=
XM_011538184.1:c.1220+206G= XP_011536486.1:n.1220+206G=
XM_011538185.1:c.856-1326G= XP_011536487.1:n.856-1326G=
XM_011538186.1:c.336G= XP_011536488.1:p.Met112=
NM_001164690.2:c.1161G= NP_001158162.1:p.Met387=
NM_001164691.2:c.1140+226G= NP_001158163.1:n.1140+226G=
NM_020547.3:c.1161G= MANE Select NP_065434.1:p.Met387=
XM_011538183.2:c.1200+226G= XP_011536485.1:n.1200+226G=
XM_011538184.2:c.1220+206G= XP_011536486.1:n.1220+206G=
XM_011538186.3:c.336G= XP_011536488.1:p.Met112=
XM_017019179.2:c.1221G= XP_016874668.1:p.Met407=
XM_024448938.1:c.1143+226G= XP_024304706.1:n.1143+226G=
XR_002957309.1:n.1129G=
XR_002957310.1:n.1108+226G=
XR_002957311.1:n.1129G=
XR_002957312.1:n.1108+226G=