Canonical Allele Identifier: CA301768847
Gene: BCL2 HGNC NCBI

Linked Data

dbSNP Id: rs184218514

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63279809A>C , CM000680.2:g.63279809A>C GRCh38
NC_000018.9:g.60947042A>C , CM000680.1:g.60947042A>C GRCh37
NC_000018.8:g.59098022A>C NCBI36
NG_009361.1:g.44572T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+38273T>G MANE Select ENSP00000329623.3:n.585+38273T>G
ENST00000677227.1:c.913+1078T>G ENSP00000504566.1:n.913+1078T>G
ENST00000678134.1:c.789+21853T>G ENSP00000503628.1:n.789+21853T>G
ENST00000678349.1:c.1137+37721T>G ENSP00000504190.1:n.1137+37721T>G
ENST00000333681.4:c.585+38273T>G ENSP00000329623.3:n.585+38273T>G
ENST00000398117.1:c.585+38273T>G ENSP00000381185.1:n.585+38273T>G
NM_000633.2:c.585+38273T>G NP_000624.2:n.585+38273T>G
XR_935246.1:n.2025+1078T>G
XR_935247.1:n.2025+1078T>G
XR_935248.1:n.1804+1078T>G
XR_935248.3:n.2306+1078T>G
NM_000633.3:c.585+38273T>G MANE Select NP_000624.2:n.585+38273T>G