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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.25164703C= , CM000664.2:g.25164703C=
GRCh38
NC_000002.11:g.25387572C= , CM000664.1:g.25387572C=
GRCh37
NC_000002.10:g.25241076C=
NCBI36
NG_008997.1:g.8988G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000395826.7:c.70G=
MANE Select
ENSP00000379170.2:p.Val24=
ENST00000264708.7:c.70G=
ENSP00000264708.3:p.Val24=
ENST00000380794.5:c.70G=
ENSP00000370171.1:p.Val24=
ENST00000395826.6:c.70G=
ENSP00000379170.2:p.Val24=
ENST00000405623.5:c.70G=
ENSP00000384092.1:p.Val24=
ENST00000449220.1:c.70G=
ENSP00000387993.1:p.Val24=
NM_000939.2:c.70G=
NP_000930.1:p.Val24=
NM_001035256.1:c.70G=
NP_001030333.1:p.Val24=
XM_011532917.1:c.70G=
XP_011531219.1:p.Val24=
NM_000939.3:c.70G=
NP_000930.1:p.Val24=
NM_001035256.2:c.70G=
NP_001030333.1:p.Val24=
NM_001319204.1:c.70G=
NP_001306133.1:p.Val24=
NM_001319205.1:c.70G=
NP_001306134.1:p.Val24=
NM_000939.4:c.70G=
MANE Select
NP_000930.1:p.Val24=
NM_001319204.2:c.70G=
NP_001306133.1:p.Val24=
NM_001319205.2:c.70G=
NP_001306134.1:p.Val24=
NM_001035256.3:c.70G=
NP_001030333.1:p.Val24=