Canonical Allele Identifier: CA521674470

Gene: GRHL3

Linked Data

• dbSNP Id: rs1159114462
• gnomAD v2: 1-24673950-C-T
• gnomAD v4: 1-24347460-C-T
• MyVariant Identifiers: chr1:g.24673950C>T (hg19) ; chr1:g.24347460C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24347460C>T , CM000663.2:g.24347460C>T	GRCh38
NC_000001.10:g.24673950C>T , CM000663.1:g.24673950C>T	GRCh37
NC_000001.9:g.24546537C>T	NCBI36
NG_009308.1:g.33070C>T
NG_009308.2:g.33070C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524724.6:c.1406-8C>T	ENSP00000431290.2:n.1406-8C>T
ENST00000528064.6:c.1265-8C>T	ENSP00000435130.2:n.1265-8C>T
ENST00000689444.1:c.1406-8C>T	ENSP00000509040.1:n.1406-8C>T
ENST00000690803.1:c.1265-8C>T	ENSP00000510783.1:n.1265-8C>T
ENST00000692334.1:c.1265-8C>T	ENSP00000509790.1:n.1265-8C>T
ENST00000361548.9:c.1544-8C>T MANE Select	ENSP00000354943.5:n.1544-8C>T
ENST00000236255.4:c.1559-8C>T	ENSP00000236255.4:n.1559-8C>T
ENST00000350501.9:c.1544-8C>T	ENSP00000288955.5:n.1544-8C>T
ENST00000356046.6:c.1406-8C>T	ENSP00000348333.2:n.1406-8C>T
ENST00000361548.8:c.1544-8C>T	ENSP00000354943.4:n.1544-8C>T
ENST00000528064.5:c.*1213-8C>T	ENSP00000435130.1:n.*1213-8C>T
NM_001195010.1:c.1406-8C>T	NP_001181939.1:n.1406-8C>T
NM_021180.3:c.1559-8C>T	NP_067003.2:n.1559-8C>T
NM_198173.2:c.1544-8C>T	NP_937816.1:n.1544-8C>T
NM_198174.2:c.1544-8C>T	NP_937817.3:n.1544-8C>T
XM_011541869.1:c.1406-8C>T	XP_011540171.1:n.1406-8C>T
XM_011541870.1:c.1265-8C>T	XP_011540172.1:n.1265-8C>T
XM_011541870.2:c.1265-8C>T	XP_011540172.1:n.1265-8C>T
NM_001195010.2:c.1406-8C>T	NP_001181939.1:n.1406-8C>T
NM_198173.3:c.1544-8C>T MANE Select	NP_937816.1:n.1544-8C>T
NM_198174.3:c.1544-8C>T	NP_937817.3:n.1544-8C>T
NM_021180.4:c.1559-8C>T	NP_067003.2:n.1559-8C>T