Canonical Allele Identifier: CA301768926

Gene: BCL2

Linked Data

• dbSNP Id: rs930820841
• MyVariant Identifiers: chr18:g.60947104G>A (hg19) ; chr18:g.63279871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63279871G>A , CM000680.2:g.63279871G>A	GRCh38
NC_000018.9:g.60947104G>A , CM000680.1:g.60947104G>A	GRCh37
NC_000018.8:g.59098084G>A	NCBI36
NG_009361.1:g.44510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.585+38211C>T MANE Select	ENSP00000329623.3:n.585+38211C>T
ENST00000677227.1:c.913+1016C>T	ENSP00000504566.1:n.913+1016C>T
ENST00000678134.1:c.789+21791C>T	ENSP00000503628.1:n.789+21791C>T
ENST00000678349.1:c.1137+37659C>T	ENSP00000504190.1:n.1137+37659C>T
ENST00000333681.4:c.585+38211C>T	ENSP00000329623.3:n.585+38211C>T
ENST00000398117.1:c.585+38211C>T	ENSP00000381185.1:n.585+38211C>T
NM_000633.2:c.585+38211C>T	NP_000624.2:n.585+38211C>T
XR_935246.1:n.2025+1016C>T
XR_935247.1:n.2025+1016C>T
XR_935248.1:n.1804+1016C>T
XR_935248.3:n.2306+1016C>T
NM_000633.3:c.585+38211C>T MANE Select	NP_000624.2:n.585+38211C>T