Canonical Allele Identifier: CA2735239493

Gene: BCL2

Linked Data

• dbSNP Id: rs2144610420

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63153350_63153353del , CM000680.2:g.63153350_63153353del	GRCh38
NC_000018.9:g.60820583_60820586del , CM000680.1:g.60820583_60820586del	GRCh37
NC_000018.8:g.58971563_58971566del	NCBI36
NG_009361.1:g.171028_171031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.586-24594_586-24591del MANE Select	ENSP00000329623.3:n.586-24594_586-24591del
ENST00000677227.1:c.914-24594_914-24591del	ENSP00000504566.1:n.914-24594_914-24591del
ENST00000678134.1:c.790-24594_790-24591del	ENSP00000503628.1:n.790-24594_790-24591del
ENST00000678301.1:c.24+4720_24+4723del	ENSP00000504546.1:n.24+4720_24+4723del
ENST00000678349.1:c.1138-24594_1138-24591del	ENSP00000504190.1:n.1138-24594_1138-24591del
ENST00000333681.4:c.586-24594_586-24591del	ENSP00000329623.3:n.586-24594_586-24591del
ENST00000398117.1:c.586-24594_586-24591del	ENSP00000381185.1:n.586-24594_586-24591del
ENST00000590515.1:n.24+8493_24+8496del
NM_000633.2:c.586-24594_586-24591del	NP_000624.2:n.586-24594_586-24591del
XR_935246.1:n.2026-24594_2026-24591del
XR_935248.1:n.1805-24594_1805-24591del
XR_935248.3:n.2307-24594_2307-24591del
NM_000633.3:c.586-24594_586-24591del MANE Select	NP_000624.2:n.586-24594_586-24591del