Canonical Allele Identifier: CA301759917

Gene: BCL2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63268814A>G , CM000680.2:g.63268814A>G	GRCh38
NC_000018.9:g.60936047A>G , CM000680.1:g.60936047A>G	GRCh37
NC_000018.8:g.59087027A>G	NCBI36
NG_009361.1:g.55567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.585+49268T>C MANE Select	ENSP00000329623.3:n.585+49268T>C
ENST00000677227.1:c.913+12073T>C	ENSP00000504566.1:n.913+12073T>C
ENST00000678134.1:c.789+32848T>C	ENSP00000503628.1:n.789+32848T>C
ENST00000678349.1:c.1137+48716T>C	ENSP00000504190.1:n.1137+48716T>C
ENST00000333681.4:c.585+49268T>C	ENSP00000329623.3:n.585+49268T>C
ENST00000398117.1:c.585+49268T>C	ENSP00000381185.1:n.585+49268T>C
NM_000633.2:c.585+49268T>C	NP_000624.2:n.585+49268T>C
XR_935246.1:n.2025+12073T>C
XR_935247.1:n.2026-9007T>C
XR_935248.1:n.1804+12073T>C
XR_935248.3:n.2306+12073T>C
NM_000633.3:c.585+49268T>C MANE Select	NP_000624.2:n.585+49268T>C