Canonical Allele Identifier: CA2036978604

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429620A= , CM000674.2:g.53429620A=	GRCh38
NC_000012.11:g.53823404A= , CM000674.1:g.53823404A=	GRCh37
NC_000012.10:g.52109671A=	NCBI36
NG_015981.1:g.10766A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1135A= MANE Select	ENSP00000257863.3:p.Met379=
ENST00000257863.8:c.1135A=	ENSP00000257863.3:p.Met379=
ENST00000379791.7:c.1135A=	ENSP00000369117.3:p.Met379=
ENST00000550311.5:c.1135A=	ENSP00000446661.1:p.Met379=
ENST00000550839.1:c.226A=	ENSP00000455338.1:p.Met76=
ENST00000552233.5:n.518A=
NM_001164690.1:c.1135A=	NP_001158162.1:p.Met379=
NM_001164691.1:c.1135A=	NP_001158163.1:p.Met379=
NM_020547.2:c.1135A=	NP_065434.1:p.Met379=
XM_011538173.1:c.1195A=	XP_011536475.1:p.Met399=
XM_011538174.1:c.1192A=	XP_011536476.1:p.Met398=
XM_011538175.1:c.1177A=	XP_011536477.1:p.Met393=
XM_011538176.1:c.1138A=	XP_011536478.1:p.Met380=
XM_011538177.1:c.1117A=	XP_011536479.1:p.Met373=
XM_011538178.1:c.976A=	XP_011536480.1:p.Met326=
XM_011538179.1:c.1195A=	XP_011536481.1:p.Met399=
XM_011538180.1:c.862A=	XP_011536482.1:p.Met288=
XM_011538181.1:c.859A=	XP_011536483.1:p.Met287=
XM_011538182.1:c.784A=	XP_011536484.1:p.Met262=
XM_011538183.1:c.1195A=	XP_011536485.1:p.Met399=
XM_011538184.1:c.1195A=	XP_011536486.1:p.Met399=
XM_011538185.1:c.856-1557A=	XP_011536487.1:n.856-1557A=
XM_011538186.1:c.310A=	XP_011536488.1:p.Met104=
NM_001164690.2:c.1135A=	NP_001158162.1:p.Met379=
NM_001164691.2:c.1135A=	NP_001158163.1:p.Met379=
NM_020547.3:c.1135A= MANE Select	NP_065434.1:p.Met379=
XM_011538183.2:c.1195A=	XP_011536485.1:p.Met399=
XM_011538184.2:c.1195A=	XP_011536486.1:p.Met399=
XM_011538186.3:c.310A=	XP_011536488.1:p.Met104=
XM_017019179.2:c.1195A=	XP_016874668.1:p.Met399=
XM_024448938.1:c.1138A=	XP_024304706.1:p.Met380=
XR_002957309.1:n.1103A=
XR_002957310.1:n.1103A=
XR_002957311.1:n.1103A=
XR_002957312.1:n.1103A=