Canonical Allele Identifier: CA372828779

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5081852A>T , CM000671.2:g.5081852A>T GRCh38
NC_000009.11:g.5081852A>T , CM000671.1:g.5081852A>T GRCh37
NC_000009.10:g.5071852A>T NCBI36
NG_009904.1:g.101608A>T , LRG_612:g.101608A>T
NG_046969.1:g.108859T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381652.4:c.2562A>T (JAK2) MANE Select ENSP00000371067.4:p.Gln854His
ENST00000381652.3:c.2562A>T (JAK2) ENSP00000371067.3:p.Gln854His
NM_004972.3:c.2562A>T , LRG_612t1:c.2562A>T (JAK2) NP_004963.1:p.Gln854His
XM_011517701.1:c.377-66508T>A (INSL6) XP_011516003.1:n.377-66508T>A
XM_011517702.1:c.376+82327T>A (INSL6) XP_011516004.1:n.376+82327T>A
XR_929169.1:n.485-66508T>A (INSL6)
NM_001322194.1:c.2562A>T (JAK2) NP_001309123.1:p.Gln854His
NM_001322195.1:c.2562A>T (JAK2) NP_001309124.1:p.Gln854His
NM_001322196.1:c.2562A>T (JAK2) NP_001309125.1:p.Gln854His
NM_001322198.1:c.1347A>T (JAK2) NP_001309127.1:p.Gln449His
NM_001322199.1:c.1347A>T (JAK2) NP_001309128.1:p.Gln449His
NM_001322204.1:c.2115A>T (JAK2) NP_001309133.1:p.Gln705His
XM_011517702.3:c.376+82327T>A (INSL6) XP_011516004.1:n.376+82327T>A
NM_004972.4:c.2562A>T (JAK2) MANE Select NP_004963.1:p.Gln854His
NM_001322194.2:c.2562A>T (JAK2) NP_001309123.1:p.Gln854His
NM_001322195.2:c.2562A>T (JAK2) NP_001309124.1:p.Gln854His
NM_001322196.2:c.2562A>T (JAK2) NP_001309125.1:p.Gln854His
NM_001322198.2:c.1347A>T (JAK2) NP_001309127.1:p.Gln449His
NM_001322199.2:c.1347A>T (JAK2) NP_001309128.1:p.Gln449His
NM_001322204.2:c.2115A>T (JAK2) NP_001309133.1:p.Gln705His
NR_169763.1:n.3046A>T (JAK2)
NR_169764.1:n.2963A>T (JAK2)