Canonical Allele Identifier: CA13613740
Gene: ETV6 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11702839G>A , CM000674.2:g.11702839G>A GRCh38
NC_000012.11:g.11855773G>A , CM000674.1:g.11855773G>A GRCh37
NC_000012.10:g.11747040G>A NCBI36
NG_011443.1:g.57986G>A , LRG_609:g.57986G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.34-49611G>A MANE Select ENSP00000379658.3:n.34-49611G>A
ENST00000396373.8:c.34-49611G>A ENSP00000379658.3:n.34-49611G>A
ENST00000541426.1:n.218-49611G>A
ENST00000544715.1:n.151-13748G>A
NM_001987.4:c.34-49611G>A , LRG_609t1:c.34-49611G>A NP_001978.1:n.34-49611G>A
XM_011520607.1:c.34-49614G>A XP_011518909.1:n.34-49614G>A
XM_011520611.1:c.-102+52679G>A XP_011518913.1:n.-102+52679G>A
XM_011520607.2:c.34-49614G>A XP_011518909.1:n.34-49614G>A
XM_011520611.2:c.-102+52679G>A XP_011518913.1:n.-102+52679G>A
XM_017018990.1:c.34-49611G>A XP_016874479.1:n.34-49611G>A
XM_017018991.1:c.-1627-49611G>A XP_016874480.1:n.-1627-49611G>A
NM_001987.5:c.34-49611G>A MANE Select NP_001978.1:n.34-49611G>A
Search 100 bp 5'
Search 100 bp 3'