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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.13691817A= , CM000667.2:g.13691817A=
GRCh38
NC_000005.9:g.13691926A= , CM000667.1:g.13691926A=
GRCh37
NC_000005.8:g.13744926A=
NCBI36
NG_013081.1:g.257664T=
NG_013081.2:g.257664T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000683611.1:n.1375T=
ENST00000265104.5:c.*167T=
MANE Select
ENSP00000265104.4:n.*167T=
ENST00000681290.1:c.*167T=
ENSP00000505288.1:n.*167T=
ENST00000265104.4:c.*167T=
ENSP00000265104.4:n.*167T=
NM_001369.2:c.*167T=
NP_001360.1:n.*167T=
XM_005248262.2:c.*167T=
XP_005248319.1:n.*167T=
XM_005248262.3:c.*167T=
XP_005248319.2:n.*167T=
XM_017009177.1:c.*167T=
XP_016864666.1:n.*167T=
XM_017009178.1:c.*167T=
XP_016864667.1:n.*167T=
XM_017009179.2:c.*167T=
XP_016864668.1:n.*167T=
XM_017009185.1:c.*167T=
XP_016864674.1:n.*167T=
XM_017009186.1:c.*167T=
XP_016864675.1:n.*167T=
XM_017009188.1:c.*167T=
XP_016864677.1:n.*167T=
XM_024454388.1:c.*167T=
XP_024310156.1:n.*167T=
XM_024454389.1:c.*167T=
XP_024310157.1:n.*167T=
NM_001369.3:c.*167T=
MANE Select
NP_001360.1:n.*167T=