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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.49022444A>C , CM000665.2:g.49022444A>C
GRCh38
NC_000003.11:g.49059877A>C , CM000665.1:g.49059877A>C
GRCh37
NC_000003.10:g.49034881A>C
NCBI36
NG_012091.1:g.11999T>G
NG_016282.1:g.6970A>C
NG_033126.1:g.3628T>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000326925.11:c.176A>C
MANE Select
ENSP00000323076.5:p.Tyr59Ser
ENST00000326912.8:c.5A>C
ENSP00000323003.4:p.Tyr2Ser
ENST00000326925.10:c.176A>C
ENSP00000323076.5:p.Tyr59Ser
ENST00000395458.6:c.5A>C
ENSP00000378843.2:p.Tyr2Ser
ENST00000451378.2:c.5A>C
ENSP00000402465.2:p.Tyr2Ser
ENST00000480392.1:n.200A>C
ENST00000496152.1:n.332A>C
NM_199069.1:c.176A>C
NP_951032.1:p.Tyr59Ser
NM_199070.1:c.5A>C
NP_951033.1:p.Tyr2Ser
NM_199073.1:c.5A>C
NP_951047.1:p.Tyr2Ser
NM_199074.1:c.5A>C
NP_951056.1:p.Tyr2Ser
NM_199069.2:c.176A>C
MANE Select
NP_951032.1:p.Tyr59Ser
NM_199070.2:c.5A>C
NP_951033.1:p.Tyr2Ser
NM_199073.2:c.5A>C
NP_951047.1:p.Tyr2Ser
NM_199074.2:c.5A>C
NP_951056.1:p.Tyr2Ser