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Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.43077257C= , CM000672.2:g.43077257C=
GRCh38
NC_000010.10:g.43572705C= , CM000672.1:g.43572705C=
GRCh37
NC_000010.9:g.42892711C=
NCBI36
NG_007489.1:g.5189C= , LRG_518:g.5189C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000615310.5:c.-2C=
ENSP00000480088.2:n.-2C=
ENST00000340058.6:c.-2C=
ENSP00000344798.4:n.-2C=
ENST00000355710.8:c.-2C=
MANE Select
ENSP00000347942.3:n.-2C=
ENST00000671844.1:c.-2C=
ENSP00000500541.1:n.-2C=
ENST00000672389.1:c.-2C=
ENSP00000500252.1:n.-2C=
ENST00000340058.5:c.-2C=
ENSP00000344798.4:n.-2C=
ENST00000355710.7:c.-2C=
ENSP00000347942.3:n.-2C=
ENST00000498820.5:c.-2C=
ENSP00000419080.1:n.-2C=
ENST00000615310.4:c.-2C=
ENSP00000480088.1:n.-2C=
NM_020630.4:c.-2C= , LRG_518t2:c.-2C=
NP_065681.1:n.-2C=
NM_020975.4:c.-2C= , LRG_518t1:c.-2C=
NP_066124.1:n.-2C=
XM_011540027.1:c.-2C=
XP_011538329.1:n.-2C=
NM_020630.5:c.-2C=
NP_065681.1:n.-2C=
NM_020975.5:c.-2C=
NP_066124.1:n.-2C=
NM_020975.6:c.-2C=
MANE Select
NP_066124.1:n.-2C=
NM_020630.6:c.-2C=
NP_065681.1:n.-2C=