Canonical Allele Identifier: CA371643255

Gene: GRHL2

Linked Data

• MyVariant Identifiers: chr8:g.102555578C>G (hg19) ; chr8:g.101543350C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543350C>G , CM000670.2:g.101543350C>G	GRCh38
NC_000008.10:g.102555578C>G , CM000670.1:g.102555578C>G	GRCh37
NC_000008.9:g.102624754C>G	NCBI36
NG_011971.1:g.55911C>G
NG_011971.2:g.55911C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.130C>G MANE Select	ENSP00000495564.1:p.Leu44Val
ENST00000251808.7:c.130C>G	ENSP00000251808.3:p.Leu44Val
ENST00000395927.1:c.82C>G	ENSP00000379260.1:p.Leu28Val
ENST00000472106.2:n.458C>G
NM_024915.3:c.130C>G	NP_079191.2:p.Leu44Val
XM_011517305.1:c.82C>G	XP_011515607.1:p.Leu28Val
XM_011517306.1:c.82C>G	XP_011515608.1:p.Leu28Val
XM_011517307.1:c.130C>G	XP_011515609.1:p.Leu44Val
NM_001330593.1:c.82C>G	NP_001317522.1:p.Leu28Val
XM_011517306.3:c.82C>G	XP_011515608.1:p.Leu28Val
XM_011517307.3:c.130C>G	XP_011515609.1:p.Leu44Val
NM_001330593.2:c.82C>G	NP_001317522.1:p.Leu28Val
NM_024915.4:c.130C>G MANE Select	NP_079191.2:p.Leu44Val