Canonical Allele Identifier: CA2308692343
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63257737C>G , CM000680.2:g.63257737C>G GRCh38
NC_000018.9:g.60924970C>G , CM000680.1:g.60924970C>G GRCh37
NC_000018.8:g.59075950C>G NCBI36
NG_009361.1:g.66644G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+60345G>C MANE Select ENSP00000329623.3:n.585+60345G>C
ENST00000677227.1:c.913+23150G>C ENSP00000504566.1:n.913+23150G>C
ENST00000678134.1:c.789+43925G>C ENSP00000503628.1:n.789+43925G>C
ENST00000678349.1:c.1137+59793G>C ENSP00000504190.1:n.1137+59793G>C
ENST00000333681.4:c.585+60345G>C ENSP00000329623.3:n.585+60345G>C
ENST00000398117.1:c.585+60345G>C ENSP00000381185.1:n.585+60345G>C
NM_000633.2:c.585+60345G>C NP_000624.2:n.585+60345G>C
XR_935246.1:n.2025+23150G>C
XR_935248.1:n.1804+23150G>C
XR_935248.3:n.2306+23150G>C
NM_000633.3:c.585+60345G>C MANE Select NP_000624.2:n.585+60345G>C