Canonical Allele Identifier: CA9610834
Community Standard Title: NM_001985.3(ETFB):c.216+1G>C
Gene: ETFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51354149C>G , CM000681.2:g.51354149C>G GRCh38
NC_000019.9:g.51857403C>G , CM000681.1:g.51857403C>G GRCh37
NC_000019.8:g.56549215C>G NCBI36
NG_007115.1:g.17270G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001985.3:c.216+1G>C MANE Select NP_001976.1:n.216+1G>C
ENST00000309244.9:c.216+1G>C MANE Select ENSP00000311930.3:n.216+1G>C
NM_001014763.1:c.489+1G>C NP_001014763.1:n.489+1G>C
NM_001985.2:c.216+1G>C NP_001976.1:n.216+1G>C
ENST00000309244.8:c.216+1G>C ENSP00000311930.3:n.216+1G>C
ENST00000354232.8:c.489+1G>C ENSP00000346173.3:n.489+1G>C
ENST00000593992.1:n.239+1G>C
ENST00000596253.1:c.216+1G>C ENSP00000469628.1:n.216+1G>C
ENST00000600067.1:c.*142+1G>C ENSP00000469452.1:n.*142+1G>C
XM_024451418.1:c.105+1G>C XP_024307186.1:n.105+1G>C