Canonical Allele Identifier: CA2580607555
Community Standard Title: NM_000633.3(BCL2):c.-717C>G
Gene: BCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63319604G>C , CM000680.2:g.63319604G>C GRCh38
NC_000018.9:g.60986837G>C , CM000680.1:g.60986837G>C GRCh37
NC_000018.8:g.59137817G>C NCBI36
NG_009361.1:g.4777C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000633.3:c.-717C>G MANE Select NP_000624.2:n.-717C>G
ENST00000333681.5:c.-717C>G MANE Select ENSP00000329623.3:n.-717C>G
NM_000657.3:c.-717C>G NP_000648.2:n.-717C>G
ENST00000333681.4:c.-717C>G ENSP00000329623.3:n.-717C>G
ENST00000398117.1:c.-938C>G ENSP00000381185.1:n.-938C>G
XM_011526135.1:c.-938C>G XP_011524437.1:n.-938C>G
XM_011526135.3:c.-938C>G XP_011524437.1:n.-938C>G
XM_017025917.2:c.-717C>G XP_016881406.1:n.-717C>G
XR_935246.1:n.175C>G
XR_935247.1:n.175C>G
XR_935248.1:n.175C>G
XR_935248.3:n.677C>G
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