Canonical Allele Identifier: CA588146128

Gene: NPR2

Linked Data

• dbSNP Id: rs1257067318
• gnomAD v2: 9-35792403-C-A
• gnomAD v4: 9-35792406-C-A
• MyVariant Identifiers: chr9:g.35792403C>A (hg19) ; chr9:g.35792406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35792406C>A , CM000671.2:g.35792406C>A	GRCh38
NC_000009.11:g.35792403C>A , CM000671.1:g.35792403C>A	GRCh37
NC_000009.10:g.35782403C>A	NCBI36
NG_009249.1:g.4998C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000685871.1:c.-3C>A	ENSP00000509964.1:n.-3C>A
ENST00000686159.1:n.74-37C>A
ENST00000687625.1:n.164+1240C>A
ENST00000688201.1:n.67-37C>A
ENST00000688869.1:n.79C>A
ENST00000692380.1:n.164+1240C>A
ENST00000342694.7:c.-3C>A MANE Select	ENSP00000341083.2:n.-3C>A
ENST00000342694.6:c.-3C>A	ENSP00000341083.2:n.-3C>A
XM_005251478.3:c.-3C>A	XP_005251535.1:n.-3C>A
XM_005251479.3:c.-115+2066C>A	XP_005251536.1:n.-115+2066C>A
XM_006716778.2:c.-3C>A	XP_006716841.1:n.-3C>A
XM_011517889.1:c.-115+2066C>A	XP_011516191.1:n.-115+2066C>A
XM_011517890.1:c.-115+2066C>A	XP_011516192.1:n.-115+2066C>A
XM_011517891.1:c.-115+2066C>A	XP_011516193.1:n.-115+2066C>A
XM_011517892.1:c.-115+2066C>A	XP_011516194.1:n.-115+2066C>A
XM_011517893.1:c.-115+2066C>A	XP_011516195.1:n.-115+2066C>A
XM_011517894.1:c.-115+2066C>A	XP_011516196.1:n.-115+2066C>A
XM_024447556.1:c.-3C>A	XP_024303324.1:n.-3C>A
XM_024447557.1:c.-3C>A	XP_024303325.1:n.-3C>A
XM_024447558.1:c.-115+2066C>A	XP_024303326.1:n.-115+2066C>A
NM_003995.4:c.-3C>A MANE Select	NP_003986.2:n.-3C>A
NM_001378923.1:c.-3C>A	NP_001365852.1:n.-3C>A