Canonical Allele Identifier: CA4972311

Gene: JAK2 INSL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5090810C>T , CM000671.2:g.5090810C>T	GRCh38
NC_000009.11:g.5090810C>T , CM000671.1:g.5090810C>T	GRCh37
NC_000009.10:g.5080810C>T	NCBI36
NG_009904.1:g.110566C>T , LRG_612:g.110566C>T
NG_046969.1:g.99901G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004972.4:c.2958C>T (JAK2) MANE Select	NP_004963.1:p.Asn986=
ENST00000381652.4:c.2958C>T (JAK2) MANE Select	ENSP00000371067.4:p.Asn986=
NM_001322194.1:c.2958C>T (JAK2)	NP_001309123.1:p.Asn986=
NM_001322194.2:c.2958C>T (JAK2)	NP_001309123.1:p.Asn986=
NM_001322195.1:c.2958C>T (JAK2)	NP_001309124.1:p.Asn986=
NM_001322195.2:c.2958C>T (JAK2)	NP_001309124.1:p.Asn986=
NM_001322196.1:c.2958C>T (JAK2)	NP_001309125.1:p.Asn986=
NM_001322196.2:c.2958C>T (JAK2)	NP_001309125.1:p.Asn986=
NM_001322198.1:c.1743C>T (JAK2)	NP_001309127.1:p.Asn581=
NM_001322198.2:c.1743C>T (JAK2)	NP_001309127.1:p.Asn581=
NM_001322199.1:c.1743C>T (JAK2)	NP_001309128.1:p.Asn581=
NM_001322199.2:c.1743C>T (JAK2)	NP_001309128.1:p.Asn581=
NM_001322204.1:c.2511C>T (JAK2)	NP_001309133.1:p.Asn837=
NM_001322204.2:c.2511C>T (JAK2)	NP_001309133.1:p.Asn837=
NM_004972.3:c.2958C>T , LRG_612t1:c.2958C>T (JAK2)	NP_004963.1:p.Asn986=
NR_169763.1:n.3442C>T (JAK2)
NR_169764.1:n.3359C>T (JAK2)
ENST00000381652.3:c.2958C>T (JAK2)	ENSP00000371067.3:p.Asn986=
XM_011517701.1:c.376+73369G>A (INSL6)	XP_011516003.1:n.376+73369G>A
XM_011517702.1:c.376+73369G>A (INSL6)	XP_011516004.1:n.376+73369G>A
XM_011517702.3:c.376+73369G>A (INSL6)	XP_011516004.1:n.376+73369G>A
XR_929169.1:n.484+73369G>A (INSL6)