Canonical Allele Identifier: CA16353891

Linked Data

dbSNP Id: rs10974944
gnomAD v2: 9-5070831-C-G
gnomAD v3: 9-5070831-C-G
gnomAD v4: 9-5070831-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5070831C>G , CM000671.2:g.5070831C>G GRCh38
NC_000009.11:g.5070831C>G , CM000671.1:g.5070831C>G GRCh37
NC_000009.10:g.5060831C>G NCBI36
NG_009904.1:g.90587C>G , LRG_612:g.90587C>G
NG_046969.1:g.119880G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381652.4:c.1641+779C>G (JAK2) MANE Select ENSP00000371067.4:n.1641+779C>G
ENST00000636127.1:c.1641+779C>G (JAK2) ENSP00000489812.1:n.1641+779C>G
ENST00000381652.3:c.1641+779C>G (JAK2) ENSP00000371067.3:n.1641+779C>G
NM_004972.3:c.1641+779C>G , LRG_612t1:c.1641+779C>G (JAK2) NP_004963.1:n.1641+779C>G
XM_011517701.1:c.377-55487G>C (INSL6) XP_011516003.1:n.377-55487G>C
XM_011517702.1:c.377-78398G>C (INSL6) XP_011516004.1:n.377-78398G>C
XR_929169.1:n.485-55487G>C (INSL6)
NM_001322194.1:c.1641+779C>G (JAK2) NP_001309123.1:n.1641+779C>G
NM_001322195.1:c.1641+779C>G (JAK2) NP_001309124.1:n.1641+779C>G
NM_001322196.1:c.1641+779C>G (JAK2) NP_001309125.1:n.1641+779C>G
NM_001322198.1:c.426+779C>G (JAK2) NP_001309127.1:n.426+779C>G
NM_001322199.1:c.426+779C>G (JAK2) NP_001309128.1:n.426+779C>G
NM_001322204.1:c.1194+779C>G (JAK2) NP_001309133.1:n.1194+779C>G
XM_011517702.3:c.377-78398G>C (INSL6) XP_011516004.1:n.377-78398G>C
NM_004972.4:c.1641+779C>G (JAK2) MANE Select NP_004963.1:n.1641+779C>G
NM_001322194.2:c.1641+779C>G (JAK2) NP_001309123.1:n.1641+779C>G
NM_001322195.2:c.1641+779C>G (JAK2) NP_001309124.1:n.1641+779C>G
NM_001322196.2:c.1641+779C>G (JAK2) NP_001309125.1:n.1641+779C>G
NM_001322198.2:c.426+779C>G (JAK2) NP_001309127.1:n.426+779C>G
NM_001322199.2:c.426+779C>G (JAK2) NP_001309128.1:n.426+779C>G
NM_001322204.2:c.1194+779C>G (JAK2) NP_001309133.1:n.1194+779C>G
NR_169763.1:n.2125+779C>G (JAK2)
NR_169764.1:n.2042+779C>G (JAK2)