Canonical Allele Identifier: CA1905675914
Gene: BMS1 HGNC NCBI

Linked Data

dbSNP Id: rs1589138851

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42798126G>T , CM000672.2:g.42798126G>T GRCh38
NC_000010.10:g.43293574G>T , CM000672.1:g.43293574G>T GRCh37
NC_000010.9:g.42613580G>T NCBI36
NG_046921.1:g.20621G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374518.6:c.2090-342G>T MANE Select ENSP00000363642.4:n.2090-342G>T
ENST00000374518.5:c.2090-342G>T ENSP00000363642.4:n.2090-342G>T
NM_014753.3:c.2090-342G>T NP_055568.3:n.2090-342G>T
XM_005271846.2:c.2090-342G>T XP_005271903.1:n.2090-342G>T
XM_005271847.2:c.1901-342G>T XP_005271904.1:n.1901-342G>T
XM_005271848.2:c.2090-342G>T XP_005271905.1:n.2090-342G>T
XM_005271849.2:c.2090-342G>T XP_005271906.1:n.2090-342G>T
XM_006718081.2:c.2090-342G>T XP_006718144.1:n.2090-342G>T
XM_011540402.1:c.2090-342G>T XP_011538704.1:n.2090-342G>T
XM_011540403.1:c.857-342G>T XP_011538705.1:n.857-342G>T
XR_246522.1:n.2179-342G>T
XR_428728.2:n.2179-342G>T
XM_005271846.3:c.2090-342G>T XP_005271903.1:n.2090-342G>T
XM_005271848.3:c.2090-342G>T XP_005271905.1:n.2090-342G>T
XM_011540402.2:c.2090-342G>T XP_011538704.1:n.2090-342G>T
XM_011540403.2:c.857-342G>T XP_011538705.1:n.857-342G>T
XR_001747266.1:n.2179-342G>T
XR_002957049.1:n.2179-342G>T
NM_014753.4:c.2090-342G>T MANE Select NP_055568.3:n.2090-342G>T