Canonical Allele Identifier: CA2735239468

Gene: BCL2

Linked Data

• dbSNP Id: rs2144610407

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153346_63153348del , CM000680.2:g.63153346_63153348del	GRCh38
NC_000018.9:g.60820579_60820581del , CM000680.1:g.60820579_60820581del	GRCh37
NC_000018.8:g.58971559_58971561del	NCBI36
NG_009361.1:g.171034_171036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24588_586-24586del MANE Select	ENSP00000329623.3:n.586-24588_586-24586del
ENST00000677227.1:c.914-24588_914-24586del	ENSP00000504566.1:n.914-24588_914-24586del
ENST00000678134.1:c.790-24588_790-24586del	ENSP00000503628.1:n.790-24588_790-24586del
ENST00000678301.1:c.24+4726_24+4728del	ENSP00000504546.1:n.24+4726_24+4728del
ENST00000678349.1:c.1138-24588_1138-24586del	ENSP00000504190.1:n.1138-24588_1138-24586del
ENST00000333681.4:c.586-24588_586-24586del	ENSP00000329623.3:n.586-24588_586-24586del
ENST00000398117.1:c.586-24588_586-24586del	ENSP00000381185.1:n.586-24588_586-24586del
ENST00000590515.1:n.24+8499_24+8501del
NM_000633.2:c.586-24588_586-24586del	NP_000624.2:n.586-24588_586-24586del
XR_935246.1:n.2026-24588_2026-24586del
XR_935248.1:n.1805-24588_1805-24586del
XR_935248.3:n.2307-24588_2307-24586del
NM_000633.3:c.586-24588_586-24586del MANE Select	NP_000624.2:n.586-24588_586-24586del