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Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.2656100C>G , CM000680.2:g.2656100C>G
GRCh38
NC_000018.9:g.2656099C>G , CM000680.1:g.2656099C>G
GRCh37
NC_000018.8:g.2646099C>G
NCBI36
NG_031972.1:g.5214C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000684915.1:n.182C>G
ENST00000688342.1:c.25C>G
ENSP00000508422.1:p.Pro9Ala
ENST00000320876.11:c.25C>G
MANE Select
ENSP00000326603.7:p.Pro9Ala
ENST00000320876.10:c.25C>G
ENSP00000326603.6:p.Pro9Ala
NM_015295.2:c.25C>G
NP_056110.2:p.Pro9Ala
XM_011525642.1:c.25C>G
XP_011523944.1:p.Pro9Ala
XM_011525643.1:c.25C>G
XP_011523945.1:p.Pro9Ala
XM_011525646.1:c.25C>G
XP_011523948.1:p.Pro9Ala
XM_011525647.1:c.25C>G
XP_011523949.1:p.Pro9Ala
XR_430039.1:n.214C>G
XR_935054.1:n.214C>G
XR_935055.1:n.214C>G
XM_011525643.2:c.25C>G
XP_011523945.1:p.Pro9Ala
XM_017025684.1:c.-718C>G
XP_016881173.1:n.-718C>G
XR_001753172.1:n.214C>G
XR_001753173.1:n.214C>G
XR_001753174.1:n.214C>G
XR_001753175.1:n.214C>G
XR_001753176.1:n.214C>G
XR_001753177.1:n.214C>G
XR_001753178.1:n.214C>G
XR_001753179.1:n.214C>G
XR_935055.2:n.214C>G
NM_015295.3:c.25C>G
MANE Select
NP_056110.2:p.Pro9Ala