Canonical Allele Identifier: CA776072683

Gene: PIEZO2

Linked Data

• dbSNP Id: rs1182732478
• gnomAD v4: 18-10762845-G-C
• MyVariant Identifiers: chr18:g.10762843G>C (hg19) ; chr18:g.10762845G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10762845G>C , CM000680.2:g.10762845G>C	GRCh38
NC_000018.9:g.10762843G>C , CM000680.1:g.10762843G>C	GRCh37
NC_000018.8:g.10752843G>C	NCBI36
NG_034005.1:g.390918C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000383408.7:c.3123+77C>G	ENSP00000372900.4:n.3123+77C>G
ENST00000686869.1:n.3180+77C>G
ENST00000674853.1:c.3123+77C>G MANE Select	ENSP00000501957.1:n.3123+77C>G
ENST00000302079.10:c.3048+77C>G	ENSP00000303316.6:n.3048+77C>G
ENST00000383408.6:c.2901+77C>G	ENSP00000372900.3:n.2901+77C>G
ENST00000503781.7:c.3048+77C>G	ENSP00000421377.3:n.3048+77C>G
ENST00000580640.5:c.3123+77C>G	ENSP00000463094.1:n.3123+77C>G
ENST00000582913.5:c.3090+77C>G	ENSP00000462115.1:n.3090+77C>G
NM_022068.3:c.3048+77C>G	NP_071351.2:n.3048+77C>G
XM_011525723.1:c.3180+77C>G	XP_011524025.1:n.3180+77C>G
XM_011525724.1:c.3123+77C>G	XP_011524026.1:n.3123+77C>G
XM_011525725.1:c.3090+77C>G	XP_011524027.1:n.3090+77C>G
XM_011525726.1:c.3180+77C>G	XP_011524028.1:n.3180+77C>G
XM_011525727.1:c.3180+77C>G	XP_011524029.1:n.3180+77C>G
XM_011525723.3:c.3180+77C>G	XP_011524025.1:n.3180+77C>G
XM_011525724.3:c.3123+77C>G	XP_011524026.1:n.3123+77C>G
XM_011525725.3:c.3090+77C>G	XP_011524027.1:n.3090+77C>G
XM_011525726.3:c.3180+77C>G	XP_011524028.1:n.3180+77C>G
XM_017025918.2:c.3141+77C>G	XP_016881407.1:n.3141+77C>G
XR_001753259.2:n.4177+77C>G
NM_001378183.1:c.3123+77C>G MANE Select	NP_001365112.1:n.3123+77C>G
NM_022068.4:c.3048+77C>G	NP_071351.2:n.3048+77C>G