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Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.75765136T>C , CM000679.2:g.75765136T>C
GRCh38
NC_000017.10:g.73761217T>C , CM000679.1:g.73761217T>C
GRCh37
NC_000017.9:g.71272812T>C
NCBI36
NG_008079.1:g.5064A>G
NG_008079.2:g.5064A>G
Transcript Alleles
HGVS
Amino-acid Change
NM_000154.2:c.1A>G
MANE Select
NP_000145.1:p.Met1Val
ENST00000588479.6:c.1A>G
MANE Select
ENSP00000465930.1:p.Met1Val
NM_000154.1:c.1A>G
NP_000145.1:p.Met1Val
NM_001381985.1:c.1A>G
NP_001368914.1:p.Met1Val
ENST00000225614.6:c.1A>G
ENSP00000225614.1:p.Met1Val
ENST00000586244.1:c.1A>G
ENSP00000468288.1:p.Met1Val
ENST00000587707.2:c.1A>G
ENSP00000468341.2:p.Met1Val
ENST00000588479.5:c.1A>G
ENSP00000465930.1:p.Met1Val
ENST00000592494.1:n.22A>G
ENST00000592997.6:c.1A>G
ENSP00000464765.2:p.Met1Val