Canonical Allele Identifier: CA2308702148
Gene: BCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63279885G= , CM000680.2:g.63279885G= GRCh38
NC_000018.9:g.60947118G= , CM000680.1:g.60947118G= GRCh37
NC_000018.8:g.59098098G= NCBI36
NG_009361.1:g.44496C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+38197C= MANE Select ENSP00000329623.3:n.585+38197C=
ENST00000677227.1:c.913+1002C= ENSP00000504566.1:n.913+1002C=
ENST00000678134.1:c.789+21777C= ENSP00000503628.1:n.789+21777C=
ENST00000678349.1:c.1137+37645C= ENSP00000504190.1:n.1137+37645C=
ENST00000333681.4:c.585+38197C= ENSP00000329623.3:n.585+38197C=
ENST00000398117.1:c.585+38197C= ENSP00000381185.1:n.585+38197C=
NM_000633.2:c.585+38197C= NP_000624.2:n.585+38197C=
XR_935246.1:n.2025+1002C=
XR_935247.1:n.2025+1002C=
XR_935248.1:n.1804+1002C=
XR_935248.3:n.2306+1002C=
NM_000633.3:c.585+38197C= MANE Select NP_000624.2:n.585+38197C=
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