Canonical Allele Identifier: CA584019020
Gene: GRHL2 HGNC NCBI

Linked Data

dbSNP Id: rs1165283653

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101524077A>G , CM000670.2:g.101524077A>G GRCh38
NC_000008.10:g.102536305A>G , CM000670.1:g.102536305A>G GRCh37
NC_000008.9:g.102605481A>G NCBI36
NG_011971.1:g.36638A>G
NG_011971.2:g.36638A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646743.1:c.21-19164A>G MANE Select ENSP00000495564.1:n.21-19164A>G
ENST00000251808.7:c.21-19164A>G ENSP00000251808.3:n.21-19164A>G
ENST00000395927.1:c.-28-19164A>G ENSP00000379260.1:n.-28-19164A>G
ENST00000472106.2:n.349-19164A>G
NM_024915.3:c.21-19164A>G NP_079191.2:n.21-19164A>G
XM_011517305.1:c.-28-19164A>G XP_011515607.1:n.-28-19164A>G
XM_011517306.1:c.-28-19164A>G XP_011515608.1:n.-28-19164A>G
XM_011517307.1:c.21-19164A>G XP_011515609.1:n.21-19164A>G
NM_001330593.1:c.-28-19164A>G NP_001317522.1:n.-28-19164A>G
XM_011517306.3:c.-28-19164A>G XP_011515608.1:n.-28-19164A>G
XM_011517307.3:c.21-19164A>G XP_011515609.1:n.21-19164A>G
NM_001330593.2:c.-28-19164A>G NP_001317522.1:n.-28-19164A>G
NM_024915.4:c.21-19164A>G MANE Select NP_079191.2:n.21-19164A>G