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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.148436805C= , CM000666.2:g.148436805C=
GRCh38
NC_000004.11:g.149357957C= , CM000666.1:g.149357957C=
GRCh37
NC_000004.10:g.149577407C=
NCBI36
NG_013350.1:g.10716G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000358102.8:c.56G=
MANE Select
ENSP00000350815.3:p.Trp19=
ENST00000342437.8:c.56G=
ENSP00000343907.4:p.Trp19=
ENST00000344721.8:c.56G=
ENSP00000341390.4:p.Trp19=
ENST00000358102.7:c.56G=
ENSP00000350815.3:p.Trp19=
ENST00000511528.1:c.56G=
ENSP00000421481.1:p.Trp19=
ENST00000512865.5:c.56G=
ENSP00000423510.1:p.Trp19=
ENST00000625323.2:c.56G=
ENSP00000486719.1:p.Trp19=
NM_000901.4:c.56G=
NP_000892.2:p.Trp19=
NM_001166104.1:c.56G=
NP_001159576.1:p.Trp19=
XM_011531975.1:c.56G=
XP_011530277.1:p.Trp19=
XM_011531976.1:c.56G=
XP_011530278.1:p.Trp19=
XM_011531977.1:c.56G=
XP_011530279.1:p.Trp19=
XM_011531978.1:c.56G=
XP_011530280.1:p.Trp19=
NM_001354819.1:c.56G=
NP_001341748.1:p.Trp19=
NR_148974.1:n.419G=
XM_011531978.2:c.56G=
XP_011530280.1:p.Trp19=
NM_000901.5:c.56G=
MANE Select
NP_000892.2:p.Trp19=
NM_001166104.2:c.56G=
NP_001159576.1:p.Trp19=
NR_148974.2:n.313G=