Canonical Allele Identifier: CA1602779814

Gene: HRH2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.175682122T= , CM000667.2:g.175682122T=	GRCh38
NC_000005.9:g.175109125T= , CM000667.1:g.175109125T=	GRCh37
NC_000005.8:g.175041731T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000636584.2:c.-525-587T= MANE Select	ENSP00000489742.1:n.-525-587T=
ENST00000377291.2:c.-525-587T=	ENSP00000366506.2:n.-525-587T=
NM_001131055.1:c.-525-587T=	NP_001124527.1:n.-525-587T=
NM_022304.2:c.-1112T=	NP_071640.1:n.-1112T=
XM_005265904.2:c.-525-587T=	XP_005265961.1:n.-525-587T=
XM_006714864.2:c.-525-587T=	XP_006714927.1:n.-525-587T=
XM_006714865.2:c.-525-587T=	XP_006714928.1:n.-525-587T=
XM_011534548.1:c.-525-587T=	XP_011532850.1:n.-525-587T=
XM_011534549.1:c.-525-587T=	XP_011532851.1:n.-525-587T=
XR_245274.2:n.361-587T=
XM_005265904.3:c.-525-587T=	XP_005265961.1:n.-525-587T=
XM_006714864.4:c.-525-587T=	XP_006714927.1:n.-525-587T=
XM_006714865.3:c.-525-587T=	XP_006714928.1:n.-525-587T=
XM_011534548.3:c.-525-587T=	XP_011532850.1:n.-525-587T=
XM_011534549.3:c.-525-587T=	XP_011532851.1:n.-525-587T=
XM_017009426.2:c.-525-587T=	XP_016864915.1:n.-525-587T=
XR_245274.3:n.394-587T=
NM_001367711.1:c.-525-587T= MANE Select	NP_001354640.1:n.-525-587T=
NR_160284.1:n.86-587T=
NM_001131055.2:c.-525-587T=	NP_001124527.1:n.-525-587T=
NM_001393460.1:c.-525-587T=	NP_001380389.1:n.-525-587T=
NM_001393461.1:c.-525-587T=	NP_001380390.1:n.-525-587T=
NR_171689.1:n.85+23967T=