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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.149895199A= , CM000667.2:g.149895199A=
GRCh38
NC_000005.9:g.149274762A= , CM000667.1:g.149274762A=
GRCh37
NC_000005.8:g.149254955A=
NCBI36
NG_009102.1:g.54595T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000255266.10:c.1712T=
MANE Select
ENSP00000255266.5:p.Met571=
ENST00000255266.9:c.1712T=
ENSP00000255266.5:p.Met571=
ENST00000508173.5:n.1896T=
ENST00000613228.1:c.1469T=
ENSP00000478060.1:p.Met490=
ENST00000617647.4:c.1469T=
ENSP00000482774.1:p.Met490=
NM_000440.2:c.1712T=
NP_000431.2:p.Met571=
XM_011537648.1:c.1712T=
XP_011535950.1:p.Met571=
XM_011537649.1:c.1166T=
XP_011535951.1:p.Met389=
XM_011537650.1:c.827T=
XP_011535952.1:p.Met276=
XM_011537651.1:c.665T=
XP_011535953.1:p.Met222=
XM_011537652.1:c.635T=
XP_011535954.1:p.Met212=
XM_011537653.1:c.635T=
XP_011535955.1:p.Met212=
XM_011537654.1:c.635T=
XP_011535956.1:p.Met212=
XM_011537650.2:c.827T=
XP_011535952.1:p.Met276=
XM_011537651.2:c.665T=
XP_011535953.1:p.Met222=
XM_011537653.2:c.635T=
XP_011535955.1:p.Met212=
XM_011537654.2:c.635T=
XP_011535956.1:p.Met212=
XM_017009572.2:c.1469T=
XP_016865061.1:p.Met490=
NM_000440.3:c.1712T=
MANE Select
NP_000431.2:p.Met571=