Canonical Allele Identifier: CA2575174618

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53430017C>T , CM000674.2:g.53430017C>T	GRCh38
NC_000012.11:g.53823801C>T , CM000674.1:g.53823801C>T	GRCh37
NC_000012.10:g.52110068C>T	NCBI36
NG_015981.1:g.11163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1288+39C>T MANE Select	ENSP00000257863.3:n.1288+39C>T
ENST00000257863.8:c.1288+39C>T	ENSP00000257863.3:n.1288+39C>T
ENST00000379791.7:c.1140+392C>T	ENSP00000369117.3:n.1140+392C>T
ENST00000550311.5:c.1288+39C>T	ENSP00000446661.1:n.1288+39C>T
ENST00000550839.1:c.379+39C>T	ENSP00000455338.1:n.379+39C>T
ENST00000552233.5:n.915C>T
NM_001164690.1:c.1288+39C>T	NP_001158162.1:n.1288+39C>T
NM_001164691.1:c.1140+392C>T	NP_001158163.1:n.1140+392C>T
NM_020547.2:c.1288+39C>T	NP_065434.1:n.1288+39C>T
XM_011538173.1:c.1348+39C>T	XP_011536475.1:n.1348+39C>T
XM_011538174.1:c.1345+39C>T	XP_011536476.1:n.1345+39C>T
XM_011538175.1:c.1330+39C>T	XP_011536477.1:n.1330+39C>T
XM_011538176.1:c.1291+39C>T	XP_011536478.1:n.1291+39C>T
XM_011538177.1:c.1270+39C>T	XP_011536479.1:n.1270+39C>T
XM_011538178.1:c.1129+39C>T	XP_011536480.1:n.1129+39C>T
XM_011538179.1:c.1200+392C>T	XP_011536481.1:n.1200+392C>T
XM_011538180.1:c.1015+39C>T	XP_011536482.1:n.1015+39C>T
XM_011538181.1:c.1012+39C>T	XP_011536483.1:n.1012+39C>T
XM_011538182.1:c.937+39C>T	XP_011536484.1:n.937+39C>T
XM_011538183.1:c.1201-129C>T	XP_011536485.1:n.1201-129C>T
XM_011538184.1:c.1220+372C>T	XP_011536486.1:n.1220+372C>T
XM_011538185.1:c.856-1160C>T	XP_011536487.1:n.856-1160C>T
XM_011538186.1:c.463+39C>T	XP_011536488.1:n.463+39C>T
NM_001164690.2:c.1288+39C>T	NP_001158162.1:n.1288+39C>T
NM_001164691.2:c.1140+392C>T	NP_001158163.1:n.1140+392C>T
NM_020547.3:c.1288+39C>T MANE Select	NP_065434.1:n.1288+39C>T
XM_011538183.2:c.1201-129C>T	XP_011536485.1:n.1201-129C>T
XM_011538184.2:c.1220+372C>T	XP_011536486.1:n.1220+372C>T
XM_011538186.3:c.463+39C>T	XP_011536488.1:n.463+39C>T
XM_017019179.2:c.1348+39C>T	XP_016874668.1:n.1348+39C>T
XM_024448938.1:c.1143+392C>T	XP_024304706.1:n.1143+392C>T
XR_002957309.1:n.1256+39C>T
XR_002957310.1:n.1109-129C>T
XR_002957311.1:n.1256+39C>T
XR_002957312.1:n.1108+392C>T