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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.38798046A= , CM000666.2:g.38798046A=
GRCh38
NC_000004.11:g.38799667A= , CM000666.1:g.38799667A=
GRCh37
NC_000004.10:g.38476062A=
NCBI36
NG_016228.1:g.11746T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000308979.7:c.786T=
MANE Select
ENSP00000354932.2:p.Ile262=
ENST00000308979.6:c.786T=
ENSP00000354932.2:p.Ile262=
ENST00000502213.6:c.786T=
ENSP00000421259.1:p.Ile262=
ENST00000505744.5:n.235+2811T=
NM_003263.3:c.786T=
NP_003254.2:p.Ile262=
XM_005262662.3:c.786T=
XP_005262719.1:p.Ile262=
XM_006714028.2:c.786T=
XP_006714091.1:p.Ile262=
XM_011513742.1:c.786T=
XP_011512044.1:p.Ile262=
XM_011513743.1:c.786T=
XP_011512045.1:p.Ile262=
XM_011513744.1:c.786T=
XP_011512046.1:p.Ile262=
XM_011513745.1:c.786T=
XP_011512047.1:p.Ile262=
XR_925162.1:n.1060T=
XR_925163.1:n.1060T=
XR_925165.1:n.1060T=
XM_005262662.5:c.786T=
XP_005262719.1:p.Ile262=
XM_011513742.3:c.786T=
XP_011512044.1:p.Ile262=
XM_011513745.3:c.786T=
XP_011512047.1:p.Ile262=
XM_017008571.2:c.786T=
XP_016864060.1:p.Ile262=
XM_017008572.2:c.786T=
XP_016864061.1:p.Ile262=
XM_024454196.1:c.786T=
XP_024309964.1:p.Ile262=
XM_024454197.1:c.786T=
XP_024309965.1:p.Ile262=
XM_024454198.1:c.786T=
XP_024309966.1:p.Ile262=
XM_024454199.1:c.205+2811T=
XP_024309967.1:n.205+2811T=
XR_925163.2:n.1060T=
XR_925165.2:n.1060T=
NM_003263.4:c.786T=
MANE Select
NP_003254.2:p.Ile262=