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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.130065845T= , CM000685.2:g.130065845T=
GRCh38
NC_000023.10:g.129199820T= , CM000685.1:g.129199820T=
GRCh37
NC_000023.9:g.129027501T=
NCBI36
NG_016388.1:g.49869A= , LRG_335:g.49869A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000308167.10:c.*876A=
MANE Select
ENSP00000311280.6:n.*876A=
ENST00000308167.9:c.*876A=
ENSP00000311280.5:n.*876A=
ENST00000335997.11:c.*876A=
ENSP00000338608.7:n.*876A=
ENST00000615377.4:c.*876A=
ENSP00000478297.1:n.*876A=
NM_001127197.1:c.*876A=
NP_001120669.1:n.*876A=
NM_001421.3:c.*876A= , LRG_335t1:c.*876A=
NP_001412.1:n.*876A=
XM_005262389.2:c.*876A=
XP_005262446.1:n.*876A=
XM_011531307.1:c.*876A=
XP_011529609.1:n.*876A=
XM_011531308.1:c.*876A=
XP_011529610.1:n.*876A=
XM_005262389.3:c.*876A=
XP_005262446.1:n.*876A=
XM_011531307.3:c.*876A=
XP_011529609.1:n.*876A=
XM_011531308.3:c.*876A=
XP_011529610.1:n.*876A=
NM_001127197.2:c.*876A=
NP_001120669.1:n.*876A=
NM_001421.4:c.*876A=
MANE Select
NP_001412.1:n.*876A=