Canonical Allele Identifier: CA4972259
Community Standard Title: NM_004972.4(JAK2):c.2768G>A (p.Arg923His)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5090452G>A , CM000671.2:g.5090452G>A GRCh38
NC_000009.11:g.5090452G>A , CM000671.1:g.5090452G>A GRCh37
NC_000009.10:g.5080452G>A NCBI36
NG_009904.1:g.110208G>A , LRG_612:g.110208G>A
NG_046969.1:g.100259C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004972.4:c.2768G>A (JAK2) MANE Select NP_004963.1:p.Arg923His
ENST00000381652.4:c.2768G>A (JAK2) MANE Select ENSP00000371067.4:p.Arg923His
NM_001322194.1:c.2768G>A (JAK2) NP_001309123.1:p.Arg923His
NM_001322194.2:c.2768G>A (JAK2) NP_001309123.1:p.Arg923His
NM_001322195.1:c.2768G>A (JAK2) NP_001309124.1:p.Arg923His
NM_001322195.2:c.2768G>A (JAK2) NP_001309124.1:p.Arg923His
NM_001322196.1:c.2768G>A (JAK2) NP_001309125.1:p.Arg923His
NM_001322196.2:c.2768G>A (JAK2) NP_001309125.1:p.Arg923His
NM_001322198.1:c.1553G>A (JAK2) NP_001309127.1:p.Arg518His
NM_001322198.2:c.1553G>A (JAK2) NP_001309127.1:p.Arg518His
NM_001322199.1:c.1553G>A (JAK2) NP_001309128.1:p.Arg518His
NM_001322199.2:c.1553G>A (JAK2) NP_001309128.1:p.Arg518His
NM_001322204.1:c.2321G>A (JAK2) NP_001309133.1:p.Arg774His
NM_001322204.2:c.2321G>A (JAK2) NP_001309133.1:p.Arg774His
NM_004972.3:c.2768G>A , LRG_612t1:c.2768G>A (JAK2) NP_004963.1:p.Arg923His
NR_169763.1:n.3252G>A (JAK2)
NR_169764.1:n.3169G>A (JAK2)
ENST00000381652.3:c.2768G>A (JAK2) ENSP00000371067.3:p.Arg923His
XM_011517701.1:c.376+73727C>T (INSL6) XP_011516003.1:n.376+73727C>T
XM_011517702.1:c.376+73727C>T (INSL6) XP_011516004.1:n.376+73727C>T
XM_011517702.3:c.376+73727C>T (INSL6) XP_011516004.1:n.376+73727C>T
XR_929169.1:n.484+73727C>T (INSL6)