Canonical Allele Identifier: CA2621687154
Gene: EIF2B1 HGNC NCBI

Linked Data

gnomAD v4: 12-123630311-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123630311G>C , CM000674.2:g.123630311G>C GRCh38
NC_000012.11:g.124114858G>C , CM000674.1:g.124114858G>C GRCh37
NC_000012.10:g.122680811G>C NCBI36
NG_015862.1:g.8466C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000424014.7:c.253-26C>G MANE Select ENSP00000416250.2:n.253-26C>G
ENST00000424014.6:c.253-26C>G ENSP00000416250.2:n.253-26C>G
ENST00000452159.6:n.384-26C>G
ENST00000534960.5:c.300-26C>G
ENST00000537073.1:c.253-26C>G ENSP00000444183.1:n.253-26C>G
ENST00000539951.5:c.214-26C>G ENSP00000438060.1:n.214-26C>G
ENST00000543940.1:n.353-7C>G
NM_001414.3:c.253-26C>G NP_001405.1:n.253-26C>G
NM_001414.4:c.253-26C>G MANE Select NP_001405.1:n.253-26C>G
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