Canonical Allele Identifier: CA2769523357

Gene: HRH2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.175682140A>G , CM000667.2:g.175682140A>G	GRCh38
NC_000005.9:g.175109143A>G , CM000667.1:g.175109143A>G	GRCh37
NC_000005.8:g.175041749A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636584.2:c.-525-569A>G MANE Select	ENSP00000489742.1:n.-525-569A>G
ENST00000377291.2:c.-525-569A>G	ENSP00000366506.2:n.-525-569A>G
NM_001131055.1:c.-525-569A>G	NP_001124527.1:n.-525-569A>G
NM_022304.2:c.-1094A>G	NP_071640.1:n.-1094A>G
XM_005265904.2:c.-525-569A>G	XP_005265961.1:n.-525-569A>G
XM_006714864.2:c.-525-569A>G	XP_006714927.1:n.-525-569A>G
XM_006714865.2:c.-525-569A>G	XP_006714928.1:n.-525-569A>G
XM_011534548.1:c.-525-569A>G	XP_011532850.1:n.-525-569A>G
XM_011534549.1:c.-525-569A>G	XP_011532851.1:n.-525-569A>G
XR_245274.2:n.361-569A>G
XM_005265904.3:c.-525-569A>G	XP_005265961.1:n.-525-569A>G
XM_006714864.4:c.-525-569A>G	XP_006714927.1:n.-525-569A>G
XM_006714865.3:c.-525-569A>G	XP_006714928.1:n.-525-569A>G
XM_011534548.3:c.-525-569A>G	XP_011532850.1:n.-525-569A>G
XM_011534549.3:c.-525-569A>G	XP_011532851.1:n.-525-569A>G
XM_017009426.2:c.-525-569A>G	XP_016864915.1:n.-525-569A>G
XR_245274.3:n.394-569A>G
NM_001367711.1:c.-525-569A>G MANE Select	NP_001354640.1:n.-525-569A>G
NR_160284.1:n.86-569A>G
NM_001131055.2:c.-525-569A>G	NP_001124527.1:n.-525-569A>G
NM_001393460.1:c.-525-569A>G	NP_001380389.1:n.-525-569A>G
NM_001393461.1:c.-525-569A>G	NP_001380390.1:n.-525-569A>G
NR_171689.1:n.85+23985A>G