Canonical Allele Identifier: CA2308692935
Gene: BCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63258928A>T , CM000680.2:g.63258928A>T GRCh38
NC_000018.9:g.60926161A>T , CM000680.1:g.60926161A>T GRCh37
NC_000018.8:g.59077141A>T NCBI36
NG_009361.1:g.65453T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+59154T>A MANE Select ENSP00000329623.3:n.585+59154T>A
ENST00000677227.1:c.913+21959T>A ENSP00000504566.1:n.913+21959T>A
ENST00000678134.1:c.789+42734T>A ENSP00000503628.1:n.789+42734T>A
ENST00000678349.1:c.1137+58602T>A ENSP00000504190.1:n.1137+58602T>A
ENST00000333681.4:c.585+59154T>A ENSP00000329623.3:n.585+59154T>A
ENST00000398117.1:c.585+59154T>A ENSP00000381185.1:n.585+59154T>A
NM_000633.2:c.585+59154T>A NP_000624.2:n.585+59154T>A
XR_935246.1:n.2025+21959T>A
XR_935247.1:n.2905T>A
XR_935248.1:n.1804+21959T>A
XR_935248.3:n.2306+21959T>A
NM_000633.3:c.585+59154T>A MANE Select NP_000624.2:n.585+59154T>A