Canonical Allele Identifier: CA188419076

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5063701T>A , CM000671.2:g.5063701T>A GRCh38
NC_000009.11:g.5063701T>A , CM000671.1:g.5063701T>A GRCh37
NC_000009.10:g.5053701T>A NCBI36
NG_009904.1:g.83457T>A , LRG_612:g.83457T>A
NG_046969.1:g.127010A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381652.4:c.1057-1182T>A (JAK2) MANE Select ENSP00000371067.4:n.1057-1182T>A
ENST00000636127.1:c.1057-1182T>A (JAK2) ENSP00000489812.1:n.1057-1182T>A
ENST00000381652.3:c.1057-1182T>A (JAK2) ENSP00000371067.3:n.1057-1182T>A
NM_004972.3:c.1057-1182T>A , LRG_612t1:c.1057-1182T>A (JAK2) NP_004963.1:n.1057-1182T>A
XM_011517701.1:c.377-48357A>T (INSL6) XP_011516003.1:n.377-48357A>T
XM_011517702.1:c.377-71268A>T (INSL6) XP_011516004.1:n.377-71268A>T
XR_929169.1:n.485-48357A>T (INSL6)
NM_001322194.1:c.1057-1182T>A (JAK2) NP_001309123.1:n.1057-1182T>A
NM_001322195.1:c.1057-1182T>A (JAK2) NP_001309124.1:n.1057-1182T>A
NM_001322196.1:c.1057-1182T>A (JAK2) NP_001309125.1:n.1057-1182T>A
NM_001322198.1:c.-159-1182T>A (JAK2) NP_001309127.1:n.-159-1182T>A
NM_001322199.1:c.-159-1182T>A (JAK2) NP_001309128.1:n.-159-1182T>A
NM_001322204.1:c.610-1182T>A (JAK2) NP_001309133.1:n.610-1182T>A
XM_011517702.3:c.377-71268A>T (INSL6) XP_011516004.1:n.377-71268A>T
NM_004972.4:c.1057-1182T>A (JAK2) MANE Select NP_004963.1:n.1057-1182T>A
NM_001322194.2:c.1057-1182T>A (JAK2) NP_001309123.1:n.1057-1182T>A
NM_001322195.2:c.1057-1182T>A (JAK2) NP_001309124.1:n.1057-1182T>A
NM_001322196.2:c.1057-1182T>A (JAK2) NP_001309125.1:n.1057-1182T>A
NM_001322198.2:c.-159-1182T>A (JAK2) NP_001309127.1:n.-159-1182T>A
NM_001322199.2:c.-159-1182T>A (JAK2) NP_001309128.1:n.-159-1182T>A
NM_001322204.2:c.610-1182T>A (JAK2) NP_001309133.1:n.610-1182T>A
NR_169763.1:n.1541-1182T>A (JAK2)
NR_169764.1:n.1458-1182T>A (JAK2)