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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.92517406A= , CM000669.2:g.92517406A=
GRCh38
NC_000007.13:g.92146720A= , CM000669.1:g.92146720A=
GRCh37
NC_000007.12:g.91984656A=
NCBI36
NG_008341.1:g.16126T=
NG_008341.2:g.16126T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000248633.9:c.1109T=
MANE Select
ENSP00000248633.4:p.Ile370=
ENST00000248633.8:c.1109T=
ENSP00000248633.4:p.Ile370=
ENST00000422866.1:c.10T=
ENST00000428214.5:c.1109T=
ENSP00000394413.1:p.Ile370=
ENST00000438045.5:c.274-3439T=
ENSP00000410438.1:n.274-3439T=
ENST00000484913.5:n.1148T=
NM_000466.2:c.1109T=
NP_000457.1:p.Ile370=
NM_001282677.1:c.1109T=
NP_001269606.1:p.Ile370=
NM_001282678.1:c.485T=
NP_001269607.1:p.Ile162=
XR_242246.3:n.1205T=
XM_017012319.2:c.-558T=
XP_016867808.1:n.-558T=
XR_001744808.2:n.219T=
XR_242246.5:n.1156T=
NM_000466.3:c.1109T=
MANE Select
NP_000457.1:p.Ile370=
NM_001282677.2:c.1109T=
NP_001269606.1:p.Ile370=
NM_001282678.2:c.485T=
NP_001269607.1:p.Ile162=