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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.149182078C= , CM000665.2:g.149182078C=
GRCh38
NC_000003.11:g.148899865C= , CM000665.1:g.148899865C=
GRCh37
NC_000003.10:g.150382555C=
NCBI36
NG_011800.1:g.44968G=
NG_011800.2:g.44968G=
NG_011800.3:g.44968G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000264613.11:c.2481G=
MANE Select
ENSP00000264613.6:p.Met827=
ENST00000264613.10:c.2481G=
ENSP00000264613.6:p.Met827=
ENST00000481169.5:c.2268G=
ENSP00000418773.1:p.Met756=
ENST00000490639.5:n.2513G=
ENST00000494544.1:c.1830G=
ENSP00000420545.1:p.Met610=
NM_000096.3:c.2481G=
NP_000087.1:p.Met827=
NR_046371.1:n.2521G=
XM_006713499.2:c.2481G=
XP_006713562.1:p.Met827=
XM_006713500.2:c.2481G=
XP_006713563.1:p.Met827=
XM_006713501.2:c.2481G=
XP_006713564.1:p.Met827=
XM_006713502.2:c.2481G=
XP_006713565.1:p.Met827=
XM_011512435.1:c.2481G=
XP_011510737.1:p.Met827=
XR_427361.2:n.2739G=
XM_006713499.3:c.2481G=
XP_006713562.1:p.Met827=
XM_006713500.4:c.2481G=
XP_006713563.1:p.Met827=
XM_006713501.3:c.2481G=
XP_006713564.1:p.Met827=
XM_011512435.2:c.2481G=
XP_011510737.1:p.Met827=
XM_017005734.2:c.2481G=
XP_016861223.1:p.Met827=
XM_017005735.2:c.2481G=
XP_016861224.1:p.Met827=
XR_427361.3:n.2697G=
NM_000096.4:c.2481G=
MANE Select
NP_000087.2:p.Met827=
NR_046371.2:n.2305G=