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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.92517501T>C , CM000669.2:g.92517501T>C
GRCh38
NC_000007.13:g.92146815T>C , CM000669.1:g.92146815T>C
GRCh37
NC_000007.12:g.91984751T>C
NCBI36
NG_008341.1:g.16031A>G
NG_008341.2:g.16031A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000248633.9:c.1014A>G
MANE Select
ENSP00000248633.4:p.Leu338=
ENST00000248633.8:c.1014A>G
ENSP00000248633.4:p.Leu338=
ENST00000428214.5:c.1014A>G
ENSP00000394413.1:p.Leu338=
ENST00000438045.5:c.274-3534A>G
ENSP00000410438.1:n.274-3534A>G
ENST00000484913.5:n.1053A>G
NM_000466.2:c.1014A>G
NP_000457.1:p.Leu338=
NM_001282677.1:c.1014A>G
NP_001269606.1:p.Leu338=
NM_001282678.1:c.390A>G
NP_001269607.1:p.Leu130=
XR_242246.3:n.1110A>G
XM_017012319.2:c.-653A>G
XP_016867808.1:n.-653A>G
XR_001744808.2:n.124A>G
XR_242246.5:n.1061A>G
NM_000466.3:c.1014A>G
MANE Select
NP_000457.1:p.Leu338=
NM_001282677.2:c.1014A>G
NP_001269606.1:p.Leu338=
NM_001282678.2:c.390A>G
NP_001269607.1:p.Leu130=