Canonical Allele Identifier: CA991090415
Gene: BCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63279878T>A , CM000680.2:g.63279878T>A GRCh38
NC_000018.9:g.60947111T>A , CM000680.1:g.60947111T>A GRCh37
NC_000018.8:g.59098091T>A NCBI36
NG_009361.1:g.44503A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333681.5:c.585+38204A>T MANE Select ENSP00000329623.3:n.585+38204A>T
ENST00000677227.1:c.913+1009A>T ENSP00000504566.1:n.913+1009A>T
ENST00000678134.1:c.789+21784A>T ENSP00000503628.1:n.789+21784A>T
ENST00000678349.1:c.1137+37652A>T ENSP00000504190.1:n.1137+37652A>T
ENST00000333681.4:c.585+38204A>T ENSP00000329623.3:n.585+38204A>T
ENST00000398117.1:c.585+38204A>T ENSP00000381185.1:n.585+38204A>T
NM_000633.2:c.585+38204A>T NP_000624.2:n.585+38204A>T
XR_935246.1:n.2025+1009A>T
XR_935247.1:n.2025+1009A>T
XR_935248.1:n.1804+1009A>T
XR_935248.3:n.2306+1009A>T
NM_000633.3:c.585+38204A>T MANE Select NP_000624.2:n.585+38204A>T