Canonical Allele Identifier: CA301768890

Gene: BCL2

Linked Data

• dbSNP Id: rs112249835
• MyVariant Identifiers: chr18:g.60947088A>G (hg19) ; chr18:g.63279855A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63279855A>G , CM000680.2:g.63279855A>G	GRCh38
NC_000018.9:g.60947088A>G , CM000680.1:g.60947088A>G	GRCh37
NC_000018.8:g.59098068A>G	NCBI36
NG_009361.1:g.44526T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.585+38227T>C MANE Select	ENSP00000329623.3:n.585+38227T>C
ENST00000677227.1:c.913+1032T>C	ENSP00000504566.1:n.913+1032T>C
ENST00000678134.1:c.789+21807T>C	ENSP00000503628.1:n.789+21807T>C
ENST00000678349.1:c.1137+37675T>C	ENSP00000504190.1:n.1137+37675T>C
ENST00000333681.4:c.585+38227T>C	ENSP00000329623.3:n.585+38227T>C
ENST00000398117.1:c.585+38227T>C	ENSP00000381185.1:n.585+38227T>C
NM_000633.2:c.585+38227T>C	NP_000624.2:n.585+38227T>C
XR_935246.1:n.2025+1032T>C
XR_935247.1:n.2025+1032T>C
XR_935248.1:n.1804+1032T>C
XR_935248.3:n.2306+1032T>C
NM_000633.3:c.585+38227T>C MANE Select	NP_000624.2:n.585+38227T>C