Canonical Allele Identifier: CA182742027
Gene: GRHL2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10955255

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101524177A>G , CM000670.2:g.101524177A>G GRCh38
NC_000008.10:g.102536405A>G , CM000670.1:g.102536405A>G GRCh37
NC_000008.9:g.102605581A>G NCBI36
NG_011971.1:g.36738A>G

Transcript Alleles

HGVS Amino-acid change
NM_024915.3:c.21-19064A>G VV NP_079191.2:p.=
XM_011517305.1:c.-28-19064A>G XP_011515607.1:p.=
XM_011517306.1:c.-28-19064A>G XP_011515608.1:p.=
XM_011517307.1:c.21-19064A>G XP_011515609.1:p.=
NM_001330593.1:c.-28-19064A>G VV NP_001317522.1:p.=
XM_011517306.3:c.-28-19064A>G
XM_011517307.3:c.21-19064A>G
ENST00000251808.7:c.21-19064A>G ENSP00000251808.3:p.=
ENST00000395927.1:c.-28-19064A>G ENSP00000379260.1:p.=
ENST00000472106.2:n.349-19064A>G