Canonical Allele Identifier: CA371645492

Gene: GRHL2

Linked Data

• MyVariant Identifiers: chr8:g.102611380G>T (hg19) ; chr8:g.101599152G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101599152G>T , CM000670.2:g.101599152G>T	GRCh38
NC_000008.10:g.102611380G>T , CM000670.1:g.102611380G>T	GRCh37
NC_000008.9:g.102680556G>T	NCBI36
NG_011971.1:g.111713G>T
NG_011971.2:g.111713G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646743.1:c.1098+1G>T MANE Select	ENSP00000495564.1:n.1098+1G>T
ENST00000251808.7:c.1098+1G>T	ENSP00000251808.3:n.1098+1G>T
ENST00000395927.1:c.1050+1G>T	ENSP00000379260.1:n.1050+1G>T
NM_024915.3:c.1098+1G>T	NP_079191.2:n.1098+1G>T
XM_011517305.1:c.1050+1G>T	XP_011515607.1:n.1050+1G>T
XM_011517306.1:c.1050+1G>T	XP_011515608.1:n.1050+1G>T
XM_011517307.1:c.1098+1G>T	XP_011515609.1:n.1098+1G>T
NM_001330593.1:c.1050+1G>T	NP_001317522.1:n.1050+1G>T
XM_011517306.3:c.1050+1G>T	XP_011515608.1:n.1050+1G>T
XM_011517307.3:c.1098+1G>T	XP_011515609.1:n.1098+1G>T
NM_001330593.2:c.1050+1G>T	NP_001317522.1:n.1050+1G>T
NM_024915.4:c.1098+1G>T MANE Select	NP_079191.2:n.1098+1G>T