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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.34506790C>T , CM000671.2:g.34506790C>T
GRCh38
NC_000009.11:g.34506788C>T , CM000671.1:g.34506788C>T
GRCh37
NC_000009.10:g.34496788C>T
NCBI36
NG_008127.1:g.52978C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000242317.9:c.1227C>T
MANE Select
ENSP00000242317.4:p.Ala409=
ENST00000242317.8:c.1227C>T
ENSP00000242317.4:p.Ala409=
ENST00000470169.5:c.164C>T
ENST00000614641.4:c.1239C>T
ENSP00000480538.1:p.Ala413=
NM_001281428.1:c.1239C>T
NP_001268357.1:p.Ala413=
NM_012144.3:c.1227C>T
NP_036276.1:p.Ala409=
XM_006716758.2:c.696C>T
XP_006716821.1:p.Ala232=
XM_011517846.1:c.1239C>T
XP_011516148.1:p.Ala413=
XM_011517847.1:c.1239C>T
XP_011516149.1:p.Ala413=
XM_011517848.1:c.1239C>T
XP_011516150.1:p.Ala413=
XM_011517849.1:c.1239C>T
XP_011516151.1:p.Ala413=
XM_011517850.1:c.1239C>T
XP_011516152.1:p.Ala413=
XR_929232.1:n.1493C>T
XR_929233.1:n.1493C>T
XR_929235.1:n.1493C>T
XM_006716758.3:c.696C>T
XP_006716821.1:p.Ala232=
XM_011517846.2:c.1239C>T
XP_011516148.1:p.Ala413=
XM_011517847.3:c.1239C>T
XP_011516149.1:p.Ala413=
XM_011517848.2:c.1239C>T
XP_011516150.1:p.Ala413=
XM_011517849.2:c.1239C>T
XP_011516151.1:p.Ala413=
XM_011517850.3:c.1239C>T
XP_011516152.1:p.Ala413=
XM_017014625.2:c.1227C>T
XP_016870114.1:p.Ala409=
XR_002956774.1:n.1440C>T
XR_929232.2:n.1440C>T
XR_929233.2:n.1440C>T
NM_012144.4:c.1227C>T
MANE Select
NP_036276.1:p.Ala409=
NM_001281428.2:c.1239C>T
NP_001268357.1:p.Ala413=