Canonical Allele Identifier: CA14926457
Gene: CSF2RB HGNC NCBI
COSMIC:
COSN17596516 (not active)
MyVariant.info:
GRCh38 chr22:g.36927946C>T
GRCh37 chr22:g.37323988C>T
gnomAD v2:
22:37323988 C / T
gnomAD v3:
22:36927946 C / T
gnomAD v4:
chr22-36927946-C-T
Joint Max Group AF 0.75678827 (EAS)
Genomes Max Group AF 0.75678827 (EAS)
dbSNP:
909486
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36927946C>T , CM000684.2:g.36927946C>T GRCh38
NC_000022.10:g.37323988C>T , CM000684.1:g.37323988C>T GRCh37
NC_000022.9:g.35653934C>T NCBI36
NG_008040.1:g.19314C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403662.8:c.392-1456C>T MANE Select ENSP00000384053.3:n.392-1456C>T
ENST00000262825.9:c.392-1456C>T ENSP00000262825.6:n.392-1456C>T
ENST00000403662.7:c.392-1456C>T ENSP00000384053.3:n.392-1456C>T
ENST00000406230.5:c.392-1456C>T ENSP00000385271.1:n.392-1456C>T
ENST00000421539.1:c.152-1456C>T ENSP00000393585.1:n.152-1456C>T
NM_000395.2:c.392-1456C>T NP_000386.1:n.392-1456C>T
XM_005261340.2:c.392-1456C>T XP_005261397.1:n.392-1456C>T
XM_011529903.1:c.392-1456C>T XP_011528205.1:n.392-1456C>T
XM_011529904.1:c.392-1456C>T XP_011528206.1:n.392-1456C>T
XM_011529905.1:c.392-1456C>T XP_011528207.1:n.392-1456C>T
XM_005261340.3:c.392-1456C>T XP_005261397.1:n.392-1456C>T
XM_011529903.2:c.392-1456C>T XP_011528205.1:n.392-1456C>T
XM_011529904.2:c.392-1456C>T XP_011528206.1:n.392-1456C>T
XM_011529905.2:c.392-1456C>T XP_011528207.1:n.392-1456C>T
NM_000395.3:c.392-1456C>T MANE Select NP_000386.1:n.392-1456C>T
Search 100 bp 5'
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