Canonical Allele Identifier: CA132797317

Gene: HRH2

Linked Data

• dbSNP Id: rs950771465
• gnomAD v2: 5-175109030-G-T
• gnomAD v3: 5-175682027-G-T
• gnomAD v4: 5-175682027-G-T
• MyVariant Identifiers: chr5:g.175109030G>T (hg19) ; chr5:g.175682027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.175682027G>T , CM000667.2:g.175682027G>T	GRCh38
NC_000005.9:g.175109030G>T , CM000667.1:g.175109030G>T	GRCh37
NC_000005.8:g.175041636G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636584.2:c.-525-682G>T MANE Select	ENSP00000489742.1:n.-525-682G>T
ENST00000377291.2:c.-525-682G>T	ENSP00000366506.2:n.-525-682G>T
NM_001131055.1:c.-525-682G>T	NP_001124527.1:n.-525-682G>T
NM_022304.2:c.-1207G>T	NP_071640.1:n.-1207G>T
XM_005265904.2:c.-525-682G>T	XP_005265961.1:n.-525-682G>T
XM_006714864.2:c.-525-682G>T	XP_006714927.1:n.-525-682G>T
XM_006714865.2:c.-525-682G>T	XP_006714928.1:n.-525-682G>T
XM_011534548.1:c.-525-682G>T	XP_011532850.1:n.-525-682G>T
XM_011534549.1:c.-525-682G>T	XP_011532851.1:n.-525-682G>T
XR_245274.2:n.361-682G>T
XM_005265904.3:c.-525-682G>T	XP_005265961.1:n.-525-682G>T
XM_006714864.4:c.-525-682G>T	XP_006714927.1:n.-525-682G>T
XM_006714865.3:c.-525-682G>T	XP_006714928.1:n.-525-682G>T
XM_011534548.3:c.-525-682G>T	XP_011532850.1:n.-525-682G>T
XM_011534549.3:c.-525-682G>T	XP_011532851.1:n.-525-682G>T
XM_017009426.2:c.-525-682G>T	XP_016864915.1:n.-525-682G>T
XR_245274.3:n.394-682G>T
NM_001367711.1:c.-525-682G>T MANE Select	NP_001354640.1:n.-525-682G>T
NR_160284.1:n.86-682G>T
NM_001131055.2:c.-525-682G>T	NP_001124527.1:n.-525-682G>T
NM_001393460.1:c.-525-682G>T	NP_001380389.1:n.-525-682G>T
NM_001393461.1:c.-525-682G>T	NP_001380390.1:n.-525-682G>T
NR_171689.1:n.85+23872G>T