Canonical Allele Identifier: CA1602779839
Gene: HRH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.175682178C= , CM000667.2:g.175682178C= GRCh38
NC_000005.9:g.175109181C= , CM000667.1:g.175109181C= GRCh37
NC_000005.8:g.175041787C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000636584.2:c.-525-531C= MANE Select ENSP00000489742.1:n.-525-531C=
ENST00000377291.2:c.-525-531C= ENSP00000366506.2:n.-525-531C=
NM_001131055.1:c.-525-531C= NP_001124527.1:n.-525-531C=
NM_022304.2:c.-1056C= NP_071640.1:n.-1056C=
XM_005265904.2:c.-525-531C= XP_005265961.1:n.-525-531C=
XM_006714864.2:c.-525-531C= XP_006714927.1:n.-525-531C=
XM_006714865.2:c.-525-531C= XP_006714928.1:n.-525-531C=
XM_011534548.1:c.-525-531C= XP_011532850.1:n.-525-531C=
XM_011534549.1:c.-525-531C= XP_011532851.1:n.-525-531C=
XR_245274.2:n.361-531C=
XM_005265904.3:c.-525-531C= XP_005265961.1:n.-525-531C=
XM_006714864.4:c.-525-531C= XP_006714927.1:n.-525-531C=
XM_006714865.3:c.-525-531C= XP_006714928.1:n.-525-531C=
XM_011534548.3:c.-525-531C= XP_011532850.1:n.-525-531C=
XM_011534549.3:c.-525-531C= XP_011532851.1:n.-525-531C=
XM_017009426.2:c.-525-531C= XP_016864915.1:n.-525-531C=
XR_245274.3:n.394-531C=
NM_001367711.1:c.-525-531C= MANE Select NP_001354640.1:n.-525-531C=
NR_160284.1:n.86-531C=
NM_001131055.2:c.-525-531C= NP_001124527.1:n.-525-531C=
NM_001393460.1:c.-525-531C= NP_001380389.1:n.-525-531C=
NM_001393461.1:c.-525-531C= NP_001380390.1:n.-525-531C=
NR_171689.1:n.85+24023C=