Canonical Allele Identifier: CA1829665152

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5081788C= , CM000671.2:g.5081788C= GRCh38
NC_000009.11:g.5081788C= , CM000671.1:g.5081788C= GRCh37
NC_000009.10:g.5071788C= NCBI36
NG_009904.1:g.101544C= , LRG_612:g.101544C=
NG_046969.1:g.108923G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381652.4:c.2498C= (JAK2) MANE Select ENSP00000371067.4:p.Ser833=
ENST00000381652.3:c.2498C= (JAK2) ENSP00000371067.3:p.Ser833=
NM_004972.3:c.2498C= , LRG_612t1:c.2498C= (JAK2) NP_004963.1:p.Ser833=
XM_011517701.1:c.377-66444G= (INSL6) XP_011516003.1:n.377-66444G=
XM_011517702.1:c.376+82391G= (INSL6) XP_011516004.1:n.376+82391G=
XR_929169.1:n.485-66444G= (INSL6)
NM_001322194.1:c.2498C= (JAK2) NP_001309123.1:p.Ser833=
NM_001322195.1:c.2498C= (JAK2) NP_001309124.1:p.Ser833=
NM_001322196.1:c.2498C= (JAK2) NP_001309125.1:p.Ser833=
NM_001322198.1:c.1283C= (JAK2) NP_001309127.1:p.Ser428=
NM_001322199.1:c.1283C= (JAK2) NP_001309128.1:p.Ser428=
NM_001322204.1:c.2051C= (JAK2) NP_001309133.1:p.Ser684=
XM_011517702.3:c.376+82391G= (INSL6) XP_011516004.1:n.376+82391G=
NM_004972.4:c.2498C= (JAK2) MANE Select NP_004963.1:p.Ser833=
NM_001322194.2:c.2498C= (JAK2) NP_001309123.1:p.Ser833=
NM_001322195.2:c.2498C= (JAK2) NP_001309124.1:p.Ser833=
NM_001322196.2:c.2498C= (JAK2) NP_001309125.1:p.Ser833=
NM_001322198.2:c.1283C= (JAK2) NP_001309127.1:p.Ser428=
NM_001322199.2:c.1283C= (JAK2) NP_001309128.1:p.Ser428=
NM_001322204.2:c.2051C= (JAK2) NP_001309133.1:p.Ser684=
NR_169763.1:n.2982C= (JAK2)
NR_169764.1:n.2899C= (JAK2)