Canonical Allele Identifier: CA1829626785
Gene: JAK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4988761C= , CM000671.2:g.4988761C= GRCh38
NC_000009.11:g.4988761C= , CM000671.1:g.4988761C= GRCh37
NC_000009.10:g.4978761C= NCBI36
NG_009904.1:g.8517C= , LRG_612:g.8517C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381652.4:c.-26+2739C= MANE Select ENSP00000371067.4:n.-26+2739C=
ENST00000636127.1:c.-26+2739C= ENSP00000489812.1:n.-26+2739C=
ENST00000381652.3:c.-26+2739C= ENSP00000371067.3:n.-26+2739C=
ENST00000476574.5:n.224+2739C=
NM_004972.3:c.-26+2739C= , LRG_612t1:c.-26+2739C= NP_004963.1:n.-26+2739C=
NM_001322194.1:c.-26+2739C= NP_001309123.1:n.-26+2739C=
NM_001322195.1:c.-26+3588C= NP_001309124.1:n.-26+3588C=
NM_001322196.1:c.-26+3131C= NP_001309125.1:n.-26+3131C=
NM_001322198.1:c.-1146+2739C= NP_001309127.1:n.-1146+2739C=
NM_001322199.1:c.-1146+2739C= NP_001309128.1:n.-1146+2739C=
NM_004972.4:c.-26+2739C= MANE Select NP_004963.1:n.-26+2739C=
NM_001322194.2:c.-26+2739C= NP_001309123.1:n.-26+2739C=
NM_001322195.2:c.-26+3588C= NP_001309124.1:n.-26+3588C=
NM_001322196.2:c.-26+3131C= NP_001309125.1:n.-26+3131C=
NM_001322198.2:c.-1146+2739C= NP_001309127.1:n.-1146+2739C=
NM_001322199.2:c.-1146+2739C= NP_001309128.1:n.-1146+2739C=
NR_169763.1:n.459+2739C=
NR_169764.1:n.376+3996C=