Canonical Allele Identifier: CA2688131415

Gene: GRHL2

Linked Data

• gnomAD v4: 8-101543466-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543466T>G , CM000670.2:g.101543466T>G	GRCh38
NC_000008.10:g.102555694T>G , CM000670.1:g.102555694T>G	GRCh37
NC_000008.9:g.102624870T>G	NCBI36
NG_011971.1:g.56027T>G
NG_011971.2:g.56027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+30T>G MANE Select	ENSP00000495564.1:n.216+30T>G
ENST00000251808.7:c.216+30T>G	ENSP00000251808.3:n.216+30T>G
ENST00000395927.1:c.168+30T>G	ENSP00000379260.1:n.168+30T>G
ENST00000472106.2:n.574T>G
NM_024915.3:c.216+30T>G	NP_079191.2:n.216+30T>G
XM_011517305.1:c.168+30T>G	XP_011515607.1:n.168+30T>G
XM_011517306.1:c.168+30T>G	XP_011515608.1:n.168+30T>G
XM_011517307.1:c.216+30T>G	XP_011515609.1:n.216+30T>G
NM_001330593.1:c.168+30T>G	NP_001317522.1:n.168+30T>G
XM_011517306.3:c.168+30T>G	XP_011515608.1:n.168+30T>G
XM_011517307.3:c.216+30T>G	XP_011515609.1:n.216+30T>G
NM_001330593.2:c.168+30T>G	NP_001317522.1:n.168+30T>G
NM_024915.4:c.216+30T>G MANE Select	NP_079191.2:n.216+30T>G