Canonical Allele Identifier: CA385095070

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823635G>T (hg19) ; chr12:g.53429851G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1161G>T MANE Select	ENSP00000257863.3:p.Met387Ile
ENST00000257863.8:c.1161G>T	ENSP00000257863.3:p.Met387Ile
ENST00000379791.7:c.1140+226G>T	ENSP00000369117.3:n.1140+226G>T
ENST00000550311.5:c.1161G>T	ENSP00000446661.1:p.Met387Ile
ENST00000550839.1:c.252G>T	ENSP00000455338.1:p.Met84Ile
ENST00000552233.5:n.749G>T
NM_001164690.1:c.1161G>T	NP_001158162.1:p.Met387Ile
NM_001164691.1:c.1140+226G>T	NP_001158163.1:n.1140+226G>T
NM_020547.2:c.1161G>T	NP_065434.1:p.Met387Ile
XM_011538173.1:c.1221G>T	XP_011536475.1:p.Met407Ile
XM_011538174.1:c.1218G>T	XP_011536476.1:p.Met406Ile
XM_011538175.1:c.1203G>T	XP_011536477.1:p.Met401Ile
XM_011538176.1:c.1164G>T	XP_011536478.1:p.Met388Ile
XM_011538177.1:c.1143G>T	XP_011536479.1:p.Met381Ile
XM_011538178.1:c.1002G>T	XP_011536480.1:p.Met334Ile
XM_011538179.1:c.1200+226G>T	XP_011536481.1:n.1200+226G>T
XM_011538180.1:c.888G>T	XP_011536482.1:p.Met296Ile
XM_011538181.1:c.885G>T	XP_011536483.1:p.Met295Ile
XM_011538182.1:c.810G>T	XP_011536484.1:p.Met270Ile
XM_011538183.1:c.1200+226G>T	XP_011536485.1:n.1200+226G>T
XM_011538184.1:c.1220+206G>T	XP_011536486.1:n.1220+206G>T
XM_011538185.1:c.856-1326G>T	XP_011536487.1:n.856-1326G>T
XM_011538186.1:c.336G>T	XP_011536488.1:p.Met112Ile
NM_001164690.2:c.1161G>T	NP_001158162.1:p.Met387Ile
NM_001164691.2:c.1140+226G>T	NP_001158163.1:n.1140+226G>T
NM_020547.3:c.1161G>T MANE Select	NP_065434.1:p.Met387Ile
XM_011538183.2:c.1200+226G>T	XP_011536485.1:n.1200+226G>T
XM_011538184.2:c.1220+206G>T	XP_011536486.1:n.1220+206G>T
XM_011538186.3:c.336G>T	XP_011536488.1:p.Met112Ile
XM_017019179.2:c.1221G>T	XP_016874668.1:p.Met407Ile
XM_024448938.1:c.1143+226G>T	XP_024304706.1:n.1143+226G>T
XR_002957309.1:n.1129G>T
XR_002957310.1:n.1108+226G>T
XR_002957311.1:n.1129G>T
XR_002957312.1:n.1108+226G>T