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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.130065759C= , CM000685.2:g.130065759C=
GRCh38
NC_000023.10:g.129199734C= , CM000685.1:g.129199734C=
GRCh37
NC_000023.9:g.129027415C=
NCBI36
NG_016388.1:g.49955G= , LRG_335:g.49955G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000308167.10:c.*962G=
MANE Select
ENSP00000311280.6:n.*962G=
ENST00000308167.9:c.*962G=
ENSP00000311280.5:n.*962G=
ENST00000335997.11:c.*962G=
ENSP00000338608.7:n.*962G=
ENST00000615377.4:c.*962G=
ENSP00000478297.1:n.*962G=
NM_001127197.1:c.*962G=
NP_001120669.1:n.*962G=
NM_001421.3:c.*962G= , LRG_335t1:c.*962G=
NP_001412.1:n.*962G=
XM_005262389.2:c.*962G=
XP_005262446.1:n.*962G=
XM_011531307.1:c.*962G=
XP_011529609.1:n.*962G=
XM_011531308.1:c.*962G=
XP_011529610.1:n.*962G=
XM_005262389.3:c.*962G=
XP_005262446.1:n.*962G=
XM_011531307.3:c.*962G=
XP_011529609.1:n.*962G=
XM_011531308.3:c.*962G=
XP_011529610.1:n.*962G=
NM_001127197.2:c.*962G=
NP_001120669.1:n.*962G=
NM_001421.4:c.*962G=
MANE Select
NP_001412.1:n.*962G=