Canonical Allele Identifier: CA2036978801
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429898T= , CM000674.2:g.53429898T= GRCh38
NC_000012.11:g.53823682T= , CM000674.1:g.53823682T= GRCh37
NC_000012.10:g.52109949T= NCBI36
NG_015981.1:g.11044T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1208T= MANE Select ENSP00000257863.3:p.Met403=
ENST00000257863.8:c.1208T= ENSP00000257863.3:p.Met403=
ENST00000379791.7:c.1140+273T= ENSP00000369117.3:n.1140+273T=
ENST00000550311.5:c.1208T= ENSP00000446661.1:p.Met403=
ENST00000550839.1:c.299T= ENSP00000455338.1:p.Met100=
ENST00000552233.5:n.796T=
NM_001164690.1:c.1208T= NP_001158162.1:p.Met403=
NM_001164691.1:c.1140+273T= NP_001158163.1:n.1140+273T=
NM_020547.2:c.1208T= NP_065434.1:p.Met403=
XM_011538173.1:c.1268T= XP_011536475.1:p.Met423=
XM_011538174.1:c.1265T= XP_011536476.1:p.Met422=
XM_011538175.1:c.1250T= XP_011536477.1:p.Met417=
XM_011538176.1:c.1211T= XP_011536478.1:p.Met404=
XM_011538177.1:c.1190T= XP_011536479.1:p.Met397=
XM_011538178.1:c.1049T= XP_011536480.1:p.Met350=
XM_011538179.1:c.1200+273T= XP_011536481.1:n.1200+273T=
XM_011538180.1:c.935T= XP_011536482.1:p.Met312=
XM_011538181.1:c.932T= XP_011536483.1:p.Met311=
XM_011538182.1:c.857T= XP_011536484.1:p.Met286=
XM_011538183.1:c.1201-248T= XP_011536485.1:n.1201-248T=
XM_011538184.1:c.1220+253T= XP_011536486.1:n.1220+253T=
XM_011538185.1:c.856-1279T= XP_011536487.1:n.856-1279T=
XM_011538186.1:c.383T= XP_011536488.1:p.Met128=
NM_001164690.2:c.1208T= NP_001158162.1:p.Met403=
NM_001164691.2:c.1140+273T= NP_001158163.1:n.1140+273T=
NM_020547.3:c.1208T= MANE Select NP_065434.1:p.Met403=
XM_011538183.2:c.1201-248T= XP_011536485.1:n.1201-248T=
XM_011538184.2:c.1220+253T= XP_011536486.1:n.1220+253T=
XM_011538186.3:c.383T= XP_011536488.1:p.Met128=
XM_017019179.2:c.1268T= XP_016874668.1:p.Met423=
XM_024448938.1:c.1143+273T= XP_024304706.1:n.1143+273T=
XR_002957309.1:n.1176T=
XR_002957310.1:n.1109-248T=
XR_002957311.1:n.1176T=
XR_002957312.1:n.1108+273T=