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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.73420300A= , CM000666.2:g.73420300A=
GRCh38
NC_000004.11:g.74286017A= , CM000666.1:g.74286017A=
GRCh37
NC_000004.10:g.74504881A=
NCBI36
NG_009291.1:g.21046A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000295897.9:c.*2A=
MANE Select
ENSP00000295897.4:n.*2A=
ENST00000295897.8:c.*2A=
ENSP00000295897.4:n.*2A=
ENST00000401494.7:c.*2A=
ENSP00000384695.3:n.*2A=
ENST00000415165.6:c.*2A=
ENSP00000401820.2:n.*2A=
ENST00000476441.6:c.*1111A=
ENSP00000423727.1:n.*1111A=
ENST00000495173.1:n.140A=
ENST00000503124.5:c.*2A=
ENSP00000421027.1:n.*2A=
ENST00000505649.5:n.1379A=
ENST00000508932.5:n.222A=
ENST00000509063.5:c.1785+661A=
ENSP00000422784.1:n.1785+661A=
ENST00000511370.1:c.1365A=
ENST00000621085.4:c.*2A=
ENSP00000483421.1:n.*2A=
ENST00000621628.4:c.*2A=
ENSP00000480485.1:n.*2A=
NM_000477.5:c.*2A=
NP_000468.1:n.*2A=
NM_000477.6:c.*2A=
NP_000468.1:n.*2A=
NM_000477.7:c.*2A=
MANE Select
NP_000468.1:n.*2A=