Canonical Allele Identifier: CA463758258

Gene: JAK2 INSL6

Linked Data

• MyVariant Identifiers: chr9:g.5081822T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5081822T>C , CM000671.2:g.5081822T>C	GRCh38
NC_000009.11:g.5081822T>C , CM000671.1:g.5081822T>C	GRCh37
NC_000009.10:g.5071822T>C	NCBI36
NG_009904.1:g.101578T>C , LRG_612:g.101578T>C
NG_046969.1:g.108889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381652.4:c.2532T>C (JAK2) MANE Select	ENSP00000371067.4:p.Phe844=
ENST00000381652.3:c.2532T>C (JAK2)	ENSP00000371067.3:p.Phe844=
NM_004972.3:c.2532T>C , LRG_612t1:c.2532T>C (JAK2)	NP_004963.1:p.Phe844=
XM_011517701.1:c.377-66478A>G (INSL6)	XP_011516003.1:n.377-66478A>G
XM_011517702.1:c.376+82357A>G (INSL6)	XP_011516004.1:n.376+82357A>G
XR_929169.1:n.485-66478A>G (INSL6)
NM_001322194.1:c.2532T>C (JAK2)	NP_001309123.1:p.Phe844=
NM_001322195.1:c.2532T>C (JAK2)	NP_001309124.1:p.Phe844=
NM_001322196.1:c.2532T>C (JAK2)	NP_001309125.1:p.Phe844=
NM_001322198.1:c.1317T>C (JAK2)	NP_001309127.1:p.Phe439=
NM_001322199.1:c.1317T>C (JAK2)	NP_001309128.1:p.Phe439=
NM_001322204.1:c.2085T>C (JAK2)	NP_001309133.1:p.Phe695=
XM_011517702.3:c.376+82357A>G (INSL6)	XP_011516004.1:n.376+82357A>G
NM_004972.4:c.2532T>C (JAK2) MANE Select	NP_004963.1:p.Phe844=
NM_001322194.2:c.2532T>C (JAK2)	NP_001309123.1:p.Phe844=
NM_001322195.2:c.2532T>C (JAK2)	NP_001309124.1:p.Phe844=
NM_001322196.2:c.2532T>C (JAK2)	NP_001309125.1:p.Phe844=
NM_001322198.2:c.1317T>C (JAK2)	NP_001309127.1:p.Phe439=
NM_001322199.2:c.1317T>C (JAK2)	NP_001309128.1:p.Phe439=
NM_001322204.2:c.2085T>C (JAK2)	NP_001309133.1:p.Phe695=
NR_169763.1:n.3016T>C (JAK2)
NR_169764.1:n.2933T>C (JAK2)