Canonical Allele Identifier: CA188439121

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5084049G>A , CM000671.2:g.5084049G>A GRCh38
NC_000009.11:g.5084049G>A , CM000671.1:g.5084049G>A GRCh37
NC_000009.10:g.5074049G>A NCBI36
NG_009904.1:g.103805G>A , LRG_612:g.103805G>A
NG_046969.1:g.106662C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381652.4:c.2571+2188G>A (JAK2) MANE Select ENSP00000371067.4:n.2571+2188G>A
ENST00000381652.3:c.2571+2188G>A (JAK2) ENSP00000371067.3:n.2571+2188G>A
NM_004972.3:c.2571+2188G>A , LRG_612t1:c.2571+2188G>A (JAK2) NP_004963.1:n.2571+2188G>A
XM_011517701.1:c.377-68705C>T (INSL6) XP_011516003.1:n.377-68705C>T
XM_011517702.1:c.376+80130C>T (INSL6) XP_011516004.1:n.376+80130C>T
XR_929169.1:n.485-68705C>T (INSL6)
NM_001322194.1:c.2571+2188G>A (JAK2) NP_001309123.1:n.2571+2188G>A
NM_001322195.1:c.2571+2188G>A (JAK2) NP_001309124.1:n.2571+2188G>A
NM_001322196.1:c.2571+2188G>A (JAK2) NP_001309125.1:n.2571+2188G>A
NM_001322198.1:c.1356+2188G>A (JAK2) NP_001309127.1:n.1356+2188G>A
NM_001322199.1:c.1356+2188G>A (JAK2) NP_001309128.1:n.1356+2188G>A
NM_001322204.1:c.2124+2188G>A (JAK2) NP_001309133.1:n.2124+2188G>A
XM_011517702.3:c.376+80130C>T (INSL6) XP_011516004.1:n.376+80130C>T
NM_004972.4:c.2571+2188G>A (JAK2) MANE Select NP_004963.1:n.2571+2188G>A
NM_001322194.2:c.2571+2188G>A (JAK2) NP_001309123.1:n.2571+2188G>A
NM_001322195.2:c.2571+2188G>A (JAK2) NP_001309124.1:n.2571+2188G>A
NM_001322196.2:c.2571+2188G>A (JAK2) NP_001309125.1:n.2571+2188G>A
NM_001322198.2:c.1356+2188G>A (JAK2) NP_001309127.1:n.1356+2188G>A
NM_001322199.2:c.1356+2188G>A (JAK2) NP_001309128.1:n.1356+2188G>A
NM_001322204.2:c.2124+2188G>A (JAK2) NP_001309133.1:n.2124+2188G>A
NR_169763.1:n.3055+2188G>A (JAK2)
NR_169764.1:n.2972+2188G>A (JAK2)