Canonical Allele Identifier: CA3430056
Gene: EGR1 HGNC NCBI

Linked Data

dbSNP Id: rs11743810

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138466715C>T , CM000667.2:g.138466715C>T GRCh38
NC_000005.9:g.137802404C>T , CM000667.1:g.137802404C>T GRCh37
NC_000005.8:g.137830303C>T NCBI36
NG_021374.1:g.6224C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000239938.5:c.308-42C>T MANE Select ENSP00000239938.4:n.308-42C>T
ENST00000239938.4:c.308-42C>T ENSP00000239938.4:n.308-42C>T
NM_001964.2:c.308-42C>T NP_001955.1:n.308-42C>T
NM_001964.3:c.308-42C>T MANE Select NP_001955.1:n.308-42C>T