Canonical Allele Identifier: CA463755185

Linked Data

MyVariant Identifiers: chr9:g.5078360A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5078360A>C , CM000671.2:g.5078360A>C GRCh38
NC_000009.11:g.5078360A>C , CM000671.1:g.5078360A>C GRCh37
NC_000009.10:g.5068360A>C NCBI36
NG_009904.1:g.98116A>C , LRG_612:g.98116A>C
NG_046969.1:g.112351T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381652.4:c.2047A>C (JAK2) MANE Select ENSP00000371067.4:p.Arg683=
ENST00000636127.1:c.2047A>C (JAK2) ENSP00000489812.1:p.Arg683=
ENST00000381652.3:c.2047A>C (JAK2) ENSP00000371067.3:p.Arg683=
NM_004972.3:c.2047A>C , LRG_612t1:c.2047A>C (JAK2) NP_004963.1:p.Arg683=
XM_011517701.1:c.377-63016T>G (INSL6) XP_011516003.1:n.377-63016T>G
XM_011517702.1:c.376+85819T>G (INSL6) XP_011516004.1:n.376+85819T>G
XR_929169.1:n.485-63016T>G (INSL6)
NM_001322194.1:c.2047A>C (JAK2) NP_001309123.1:p.Arg683=
NM_001322195.1:c.2047A>C (JAK2) NP_001309124.1:p.Arg683=
NM_001322196.1:c.2047A>C (JAK2) NP_001309125.1:p.Arg683=
NM_001322198.1:c.832A>C (JAK2) NP_001309127.1:p.Arg278=
NM_001322199.1:c.832A>C (JAK2) NP_001309128.1:p.Arg278=
NM_001322204.1:c.1600A>C (JAK2) NP_001309133.1:p.Arg534=
XM_011517702.3:c.376+85819T>G (INSL6) XP_011516004.1:n.376+85819T>G
NM_004972.4:c.2047A>C (JAK2) MANE Select NP_004963.1:p.Arg683=
NM_001322194.2:c.2047A>C (JAK2) NP_001309123.1:p.Arg683=
NM_001322195.2:c.2047A>C (JAK2) NP_001309124.1:p.Arg683=
NM_001322196.2:c.2047A>C (JAK2) NP_001309125.1:p.Arg683=
NM_001322198.2:c.832A>C (JAK2) NP_001309127.1:p.Arg278=
NM_001322199.2:c.832A>C (JAK2) NP_001309128.1:p.Arg278=
NM_001322204.2:c.1600A>C (JAK2) NP_001309133.1:p.Arg534=
NR_169763.1:n.2531A>C (JAK2)
NR_169764.1:n.2448A>C (JAK2)