Canonical Allele Identifier: CA372825489

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5069933A>C , CM000671.2:g.5069933A>C GRCh38
NC_000009.11:g.5069933A>C , CM000671.1:g.5069933A>C GRCh37
NC_000009.10:g.5059933A>C NCBI36
NG_009904.1:g.89689A>C , LRG_612:g.89689A>C
NG_046969.1:g.120778T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381652.4:c.1522A>C (JAK2) MANE Select ENSP00000371067.4:p.Asn508His
ENST00000636127.1:c.1522A>C (JAK2) ENSP00000489812.1:p.Asn508His
ENST00000381652.3:c.1522A>C (JAK2) ENSP00000371067.3:p.Asn508His
NM_004972.3:c.1522A>C , LRG_612t1:c.1522A>C (JAK2) NP_004963.1:p.Asn508His
XM_011517701.1:c.377-54589T>G (INSL6) XP_011516003.1:n.377-54589T>G
XM_011517702.1:c.377-77500T>G (INSL6) XP_011516004.1:n.377-77500T>G
XR_929169.1:n.485-54589T>G (INSL6)
NM_001322194.1:c.1522A>C (JAK2) NP_001309123.1:p.Asn508His
NM_001322195.1:c.1522A>C (JAK2) NP_001309124.1:p.Asn508His
NM_001322196.1:c.1522A>C (JAK2) NP_001309125.1:p.Asn508His
NM_001322198.1:c.307A>C (JAK2) NP_001309127.1:p.Asn103His
NM_001322199.1:c.307A>C (JAK2) NP_001309128.1:p.Asn103His
NM_001322204.1:c.1075A>C (JAK2) NP_001309133.1:p.Asn359His
XM_011517702.3:c.377-77500T>G (INSL6) XP_011516004.1:n.377-77500T>G
NM_004972.4:c.1522A>C (JAK2) MANE Select NP_004963.1:p.Asn508His
NM_001322194.2:c.1522A>C (JAK2) NP_001309123.1:p.Asn508His
NM_001322195.2:c.1522A>C (JAK2) NP_001309124.1:p.Asn508His
NM_001322196.2:c.1522A>C (JAK2) NP_001309125.1:p.Asn508His
NM_001322198.2:c.307A>C (JAK2) NP_001309127.1:p.Asn103His
NM_001322199.2:c.307A>C (JAK2) NP_001309128.1:p.Asn103His
NM_001322204.2:c.1075A>C (JAK2) NP_001309133.1:p.Asn359His
NR_169763.1:n.2006A>C (JAK2)
NR_169764.1:n.1923A>C (JAK2)