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Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.50074308A= , CM000684.2:g.50074308A=
GRCh38
NC_000022.10:g.50512737A= , CM000684.1:g.50512737A=
GRCh37
NC_000022.9:g.48854864A=
NCBI36
NG_009162.1:g.16622T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000311597.10:c.622T=
MANE Select
ENSP00000310375.6:p.Ser208=
ENST00000311597.9:c.622T=
ENSP00000310375.5:p.Ser208=
ENST00000395876.6:c.622T=
ENSP00000379216.2:p.Ser208=
ENST00000442311.1:c.532T=
ENSP00000401385.1:p.Ser178=
ENST00000470008.1:n.102T=
NM_015166.3:c.622T=
NP_055981.1:p.Ser208=
NM_139202.2:c.622T=
NP_631941.1:p.Ser208=
XM_011530678.1:c.622T=
XP_011528980.1:p.Ser208=
XR_430476.2:n.1017T=
XM_011530678.2:c.622T=
XP_011528980.1:p.Ser208=
XM_017028671.1:c.622T=
XP_016884160.1:p.Ser208=
XR_001755180.2:n.1127T=
XR_001755181.2:n.895T=
NM_001376472.1:c.622T=
NP_001363401.1:p.Ser208=
NM_001376473.1:c.622T=
NP_001363402.1:p.Ser208=
NM_001376474.1:c.622T=
NP_001363403.1:p.Ser208=
NM_001376475.1:c.622T=
NP_001363404.1:p.Ser208=
NM_001376476.1:c.622T=
NP_001363405.1:p.Ser208=
NM_001376477.1:c.622T=
NP_001363406.1:p.Ser208=
NM_001376478.1:c.622T=
NP_001363407.1:p.Ser208=
NM_001376479.1:c.622T=
NP_001363408.1:p.Ser208=
NM_001376480.1:c.532T=
NP_001363409.1:p.Ser178=
NM_001376481.1:c.520T=
NP_001363410.1:p.Ser174=
NM_001376482.1:c.466T=
NP_001363411.1:p.Ser156=
NM_001376483.1:c.466T=
NP_001363412.1:p.Ser156=
NM_001376484.1:c.385T=
NP_001363413.1:p.Ser129=
NM_015166.4:c.622T=
MANE Select
NP_055981.1:p.Ser208=
NM_139202.3:c.622T=
NP_631941.1:p.Ser208=
NR_164811.1:n.969T=
NR_164812.1:n.753T=
NR_164813.1:n.1146T=