Canonical Allele Identifier: CA132797335

Gene: HRH2

Linked Data

• dbSNP Id: rs188349884
• gnomAD v2: 5-175109182-G-A
• gnomAD v3: 5-175682179-G-A
• gnomAD v4: 5-175682179-G-A
• MyVariant Identifiers: chr5:g.175109182G>A (hg19) ; chr5:g.175682179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.175682179G>A , CM000667.2:g.175682179G>A	GRCh38
NC_000005.9:g.175109182G>A , CM000667.1:g.175109182G>A	GRCh37
NC_000005.8:g.175041788G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636584.2:c.-525-530G>A MANE Select	ENSP00000489742.1:n.-525-530G>A
ENST00000377291.2:c.-525-530G>A	ENSP00000366506.2:n.-525-530G>A
NM_001131055.1:c.-525-530G>A	NP_001124527.1:n.-525-530G>A
NM_022304.2:c.-1055G>A	NP_071640.1:n.-1055G>A
XM_005265904.2:c.-525-530G>A	XP_005265961.1:n.-525-530G>A
XM_006714864.2:c.-525-530G>A	XP_006714927.1:n.-525-530G>A
XM_006714865.2:c.-525-530G>A	XP_006714928.1:n.-525-530G>A
XM_011534548.1:c.-525-530G>A	XP_011532850.1:n.-525-530G>A
XM_011534549.1:c.-525-530G>A	XP_011532851.1:n.-525-530G>A
XR_245274.2:n.361-530G>A
XM_005265904.3:c.-525-530G>A	XP_005265961.1:n.-525-530G>A
XM_006714864.4:c.-525-530G>A	XP_006714927.1:n.-525-530G>A
XM_006714865.3:c.-525-530G>A	XP_006714928.1:n.-525-530G>A
XM_011534548.3:c.-525-530G>A	XP_011532850.1:n.-525-530G>A
XM_011534549.3:c.-525-530G>A	XP_011532851.1:n.-525-530G>A
XM_017009426.2:c.-525-530G>A	XP_016864915.1:n.-525-530G>A
XR_245274.3:n.394-530G>A
NM_001367711.1:c.-525-530G>A MANE Select	NP_001354640.1:n.-525-530G>A
NR_160284.1:n.86-530G>A
NM_001131055.2:c.-525-530G>A	NP_001124527.1:n.-525-530G>A
NM_001393460.1:c.-525-530G>A	NP_001380389.1:n.-525-530G>A
NM_001393461.1:c.-525-530G>A	NP_001380390.1:n.-525-530G>A
NR_171689.1:n.85+24024G>A