Canonical Allele Identifier: CA807917406

Gene: HRH2

Linked Data

• dbSNP Id: rs1305902719
• gnomAD v3: 5-175682077-T-C
• gnomAD v4: 5-175682077-T-C
• MyVariant Identifiers: chr5:g.175109080T>C (hg19) ; chr5:g.175682077T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.175682077T>C , CM000667.2:g.175682077T>C	GRCh38
NC_000005.9:g.175109080T>C , CM000667.1:g.175109080T>C	GRCh37
NC_000005.8:g.175041686T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000636584.2:c.-525-632T>C MANE Select	ENSP00000489742.1:n.-525-632T>C
ENST00000377291.2:c.-525-632T>C	ENSP00000366506.2:n.-525-632T>C
NM_001131055.1:c.-525-632T>C	NP_001124527.1:n.-525-632T>C
NM_022304.2:c.-1157T>C	NP_071640.1:n.-1157T>C
XM_005265904.2:c.-525-632T>C	XP_005265961.1:n.-525-632T>C
XM_006714864.2:c.-525-632T>C	XP_006714927.1:n.-525-632T>C
XM_006714865.2:c.-525-632T>C	XP_006714928.1:n.-525-632T>C
XM_011534548.1:c.-525-632T>C	XP_011532850.1:n.-525-632T>C
XM_011534549.1:c.-525-632T>C	XP_011532851.1:n.-525-632T>C
XR_245274.2:n.361-632T>C
XM_005265904.3:c.-525-632T>C	XP_005265961.1:n.-525-632T>C
XM_006714864.4:c.-525-632T>C	XP_006714927.1:n.-525-632T>C
XM_006714865.3:c.-525-632T>C	XP_006714928.1:n.-525-632T>C
XM_011534548.3:c.-525-632T>C	XP_011532850.1:n.-525-632T>C
XM_011534549.3:c.-525-632T>C	XP_011532851.1:n.-525-632T>C
XM_017009426.2:c.-525-632T>C	XP_016864915.1:n.-525-632T>C
XR_245274.3:n.394-632T>C
NM_001367711.1:c.-525-632T>C MANE Select	NP_001354640.1:n.-525-632T>C
NR_160284.1:n.86-632T>C
NM_001131055.2:c.-525-632T>C	NP_001124527.1:n.-525-632T>C
NM_001393460.1:c.-525-632T>C	NP_001380389.1:n.-525-632T>C
NM_001393461.1:c.-525-632T>C	NP_001380390.1:n.-525-632T>C
NR_171689.1:n.85+23922T>C