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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38440757G= , CM000681.2:g.38440757G=
GRCh38
NC_000019.9:g.38931397G= , CM000681.1:g.38931397G=
GRCh37
NC_000019.8:g.43623237G=
NCBI36
NG_008866.1:g.12058G= , LRG_766:g.12058G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000599547.6:c.58G=
ENSP00000471601.2:p.Val20=
ENST00000359596.8:c.58G=
MANE Select
ENSP00000352608.2:p.Val20=
ENST00000355481.8:c.58G=
ENSP00000347667.3:p.Val20=
ENST00000359596.7:c.58G=
ENSP00000352608.2:p.Val20=
ENST00000360985.7:c.58G=
ENSP00000354254.4:p.Val20=
NM_000540.2:c.58G= , LRG_766t1:c.58G=
NP_000531.2:p.Val20=
NM_001042723.1:c.58G=
NP_001036188.1:p.Val20=
XM_006723317.1:c.58G=
XP_006723380.1:p.Val20=
XM_006723319.1:c.58G=
XP_006723382.1:p.Val20=
XM_011527204.1:c.58G=
XP_011525506.1:p.Val20=
XM_011527205.1:c.58G=
XP_011525507.1:p.Val20=
XM_006723317.2:c.58G=
XP_006723380.1:p.Val20=
XM_006723319.2:c.58G=
XP_006723382.1:p.Val20=
XM_011527205.2:c.58G=
XP_011525507.1:p.Val20=
XR_001753735.1:n.141G=
NM_000540.3:c.58G=
MANE Select
NP_000531.2:p.Val20=
NM_001042723.2:c.58G=
NP_001036188.1:p.Val20=