Canonical Allele Identifier: CA12734411
Gene: GRHL2 HGNC NCBI

Linked Data

dbSNP Id: rs3735714

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101667094C>T , CM000670.2:g.101667094C>T GRCh38
NC_000008.10:g.102679322C>T , CM000670.1:g.102679322C>T GRCh37
NC_000008.9:g.102748498C>T NCBI36
NG_011971.1:g.179655C>T
NG_011971.2:g.179655C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646743.1:c.*391C>T MANE Select ENSP00000495564.1:n.*391C>T
ENST00000251808.7:c.*391C>T ENSP00000251808.3:n.*391C>T
NM_024915.3:c.*391C>T NP_079191.2:n.*391C>T
XM_011517305.1:c.*391C>T XP_011515607.1:n.*391C>T
XM_011517306.1:c.*391C>T XP_011515608.1:n.*391C>T
XM_011517307.1:c.1763+2576C>T XP_011515609.1:n.1763+2576C>T
NM_001330593.1:c.*391C>T NP_001317522.1:n.*391C>T
XM_011517306.3:c.*391C>T XP_011515608.1:n.*391C>T
XM_011517307.3:c.1763+2576C>T XP_011515609.1:n.1763+2576C>T
NM_001330593.2:c.*391C>T NP_001317522.1:n.*391C>T
NM_024915.4:c.*391C>T MANE Select NP_079191.2:n.*391C>T