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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.49022443T>G , CM000665.2:g.49022443T>G
GRCh38
NC_000003.11:g.49059876T>G , CM000665.1:g.49059876T>G
GRCh37
NC_000003.10:g.49034880T>G
NCBI36
NG_012091.1:g.12000A>C
NG_016282.1:g.6969T>G
NG_033126.1:g.3629A>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000326925.11:c.175T>G
MANE Select
ENSP00000323076.5:p.Tyr59Asp
ENST00000326912.8:c.4T>G
ENSP00000323003.4:p.Tyr2Asp
ENST00000326925.10:c.175T>G
ENSP00000323076.5:p.Tyr59Asp
ENST00000395458.6:c.4T>G
ENSP00000378843.2:p.Tyr2Asp
ENST00000451378.2:c.4T>G
ENSP00000402465.2:p.Tyr2Asp
ENST00000480392.1:n.199T>G
ENST00000496152.1:n.331T>G
NM_199069.1:c.175T>G
NP_951032.1:p.Tyr59Asp
NM_199070.1:c.4T>G
NP_951033.1:p.Tyr2Asp
NM_199073.1:c.4T>G
NP_951047.1:p.Tyr2Asp
NM_199074.1:c.4T>G
NP_951056.1:p.Tyr2Asp
NM_199069.2:c.175T>G
MANE Select
NP_951032.1:p.Tyr59Asp
NM_199070.2:c.4T>G
NP_951033.1:p.Tyr2Asp
NM_199073.2:c.4T>G
NP_951047.1:p.Tyr2Asp
NM_199074.2:c.4T>G
NP_951056.1:p.Tyr2Asp