Canonical Allele Identifier: CA2619053364
Gene: AMHR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53430070C>G , CM000674.2:g.53430070C>G GRCh38
NC_000012.11:g.53823854C>G , CM000674.1:g.53823854C>G GRCh37
NC_000012.10:g.52110121C>G NCBI36
NG_015981.1:g.11216C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1289-76C>G MANE Select ENSP00000257863.3:n.1289-76C>G
ENST00000257863.8:c.1289-76C>G ENSP00000257863.3:n.1289-76C>G
ENST00000379791.7:c.1140+445C>G ENSP00000369117.3:n.1140+445C>G
ENST00000550311.5:c.1289-80C>G ENSP00000446661.1:n.1289-80C>G
ENST00000550839.1:c.380-76C>G ENSP00000455338.1:n.380-76C>G
ENST00000552233.5:n.968C>G
NM_001164690.1:c.1289-80C>G NP_001158162.1:n.1289-80C>G
NM_001164691.1:c.1140+445C>G NP_001158163.1:n.1140+445C>G
NM_020547.2:c.1289-76C>G NP_065434.1:n.1289-76C>G
XM_011538173.1:c.1349-76C>G XP_011536475.1:n.1349-76C>G
XM_011538174.1:c.1346-76C>G XP_011536476.1:n.1346-76C>G
XM_011538175.1:c.1331-76C>G XP_011536477.1:n.1331-76C>G
XM_011538176.1:c.1292-76C>G XP_011536478.1:n.1292-76C>G
XM_011538177.1:c.1271-76C>G XP_011536479.1:n.1271-76C>G
XM_011538178.1:c.1130-76C>G XP_011536480.1:n.1130-76C>G
XM_011538179.1:c.1200+445C>G XP_011536481.1:n.1200+445C>G
XM_011538180.1:c.1016-76C>G XP_011536482.1:n.1016-76C>G
XM_011538181.1:c.1013-76C>G XP_011536483.1:n.1013-76C>G
XM_011538182.1:c.938-76C>G XP_011536484.1:n.938-76C>G
XM_011538183.1:c.1201-76C>G XP_011536485.1:n.1201-76C>G
XM_011538184.1:c.1220+425C>G XP_011536486.1:n.1220+425C>G
XM_011538185.1:c.856-1107C>G XP_011536487.1:n.856-1107C>G
XM_011538186.1:c.464-76C>G XP_011536488.1:n.464-76C>G
NM_001164690.2:c.1289-80C>G NP_001158162.1:n.1289-80C>G
NM_001164691.2:c.1140+445C>G NP_001158163.1:n.1140+445C>G
NM_020547.3:c.1289-76C>G MANE Select NP_065434.1:n.1289-76C>G
XM_011538183.2:c.1201-76C>G XP_011536485.1:n.1201-76C>G
XM_011538184.2:c.1220+425C>G XP_011536486.1:n.1220+425C>G
XM_011538186.3:c.464-76C>G XP_011536488.1:n.464-76C>G
XM_017019179.2:c.1348+92C>G XP_016874668.1:n.1348+92C>G
XM_024448938.1:c.1143+445C>G XP_024304706.1:n.1143+445C>G
XR_002957309.1:n.1257-76C>G
XR_002957310.1:n.1109-76C>G
XR_002957311.1:n.1256+92C>G
XR_002957312.1:n.1108+445C>G