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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.74457330T>C , CM000673.2:g.74457330T>C
GRCh38
NC_000011.9:g.74168375T>C , CM000673.1:g.74168375T>C
GRCh37
NC_000011.8:g.73846023T>C
NCBI36
NG_011833.1:g.15226A>G , LRG_439:g.15226A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000310128.9:c.234A>G
MANE Select
ENSP00000310557.4:p.Gly78=
ENST00000310128.8:c.234A>G
ENSP00000310557.4:p.Gly78=
ENST00000525550.1:c.234A>G
ENSP00000433633.1:p.Gly78=
ENST00000532569.5:c.234A>G
ENSP00000431739.1:p.Gly78=
NM_005472.4:c.234A>G , LRG_439t1:c.234A>G
NP_005463.1:p.Gly78=
XM_011544713.1:c.366A>G
XP_011543015.1:p.Gly122=
XM_011544713.2:c.366A>G
XP_011543015.1:p.Gly122=
XM_017017047.1:c.234A>G
XP_016872536.1:p.Gly78=
XM_017017048.1:c.234A>G
XP_016872537.1:p.Gly78=
XM_017017049.1:c.234A>G
XP_016872538.1:p.Gly78=
XM_017017051.2:c.234A>G
XP_016872540.1:p.Gly78=
XM_017017052.1:c.234A>G
XP_016872541.1:p.Gly78=
NM_005472.5:c.234A>G
MANE Select
NP_005463.1:p.Gly78=