Canonical Allele Identifier: CA385095189

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823660C>A (hg19) ; chr12:g.53429876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429876C>A , CM000674.2:g.53429876C>A	GRCh38
NC_000012.11:g.53823660C>A , CM000674.1:g.53823660C>A	GRCh37
NC_000012.10:g.52109927C>A	NCBI36
NG_015981.1:g.11022C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1186C>A MANE Select	ENSP00000257863.3:p.Leu396Met
ENST00000257863.8:c.1186C>A	ENSP00000257863.3:p.Leu396Met
ENST00000379791.7:c.1140+251C>A	ENSP00000369117.3:n.1140+251C>A
ENST00000550311.5:c.1186C>A	ENSP00000446661.1:p.Leu396Met
ENST00000550839.1:c.277C>A	ENSP00000455338.1:p.Leu93Met
ENST00000552233.5:n.774C>A
NM_001164690.1:c.1186C>A	NP_001158162.1:p.Leu396Met
NM_001164691.1:c.1140+251C>A	NP_001158163.1:n.1140+251C>A
NM_020547.2:c.1186C>A	NP_065434.1:p.Leu396Met
XM_011538173.1:c.1246C>A	XP_011536475.1:p.Leu416Met
XM_011538174.1:c.1243C>A	XP_011536476.1:p.Leu415Met
XM_011538175.1:c.1228C>A	XP_011536477.1:p.Leu410Met
XM_011538176.1:c.1189C>A	XP_011536478.1:p.Leu397Met
XM_011538177.1:c.1168C>A	XP_011536479.1:p.Leu390Met
XM_011538178.1:c.1027C>A	XP_011536480.1:p.Leu343Met
XM_011538179.1:c.1200+251C>A	XP_011536481.1:n.1200+251C>A
XM_011538180.1:c.913C>A	XP_011536482.1:p.Leu305Met
XM_011538181.1:c.910C>A	XP_011536483.1:p.Leu304Met
XM_011538182.1:c.835C>A	XP_011536484.1:p.Leu279Met
XM_011538183.1:c.1200+251C>A	XP_011536485.1:n.1200+251C>A
XM_011538184.1:c.1220+231C>A	XP_011536486.1:n.1220+231C>A
XM_011538185.1:c.856-1301C>A	XP_011536487.1:n.856-1301C>A
XM_011538186.1:c.361C>A	XP_011536488.1:p.Leu121Met
NM_001164690.2:c.1186C>A	NP_001158162.1:p.Leu396Met
NM_001164691.2:c.1140+251C>A	NP_001158163.1:n.1140+251C>A
NM_020547.3:c.1186C>A MANE Select	NP_065434.1:p.Leu396Met
XM_011538183.2:c.1200+251C>A	XP_011536485.1:n.1200+251C>A
XM_011538184.2:c.1220+231C>A	XP_011536486.1:n.1220+231C>A
XM_011538186.3:c.361C>A	XP_011536488.1:p.Leu121Met
XM_017019179.2:c.1246C>A	XP_016874668.1:p.Leu416Met
XM_024448938.1:c.1143+251C>A	XP_024304706.1:n.1143+251C>A
XR_002957309.1:n.1154C>A
XR_002957310.1:n.1108+251C>A
XR_002957311.1:n.1154C>A
XR_002957312.1:n.1108+251C>A