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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173909726C= , CM000663.2:g.173909726C=
GRCh38
NC_000001.10:g.173878864C= , CM000663.1:g.173878864C=
GRCh37
NC_000001.9:g.172145487C=
NCBI36
NG_012462.1:g.12653G= , LRG_577:g.12653G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.979G=
MANE Select
ENSP00000356671.3:p.Val327=
ENST00000367698.3:c.979G=
ENSP00000356671.3:p.Val327=
ENST00000617423.4:c.559+2138G=
ENSP00000478688.1:n.559+2138G=
NM_000488.3:c.979G= , LRG_577t1:c.979G=
NP_000479.1:p.Val327=
XM_005245198.2:c.835G=
XP_005245255.1:p.Val279=
NM_001365052.1:c.835G=
NP_001351981.1:p.Val279=
NM_000488.4:c.979G=
MANE Select
NP_000479.1:p.Val327=
NM_001365052.2:c.835G=
NP_001351981.1:p.Val279=
NM_001386302.1:c.1102G=
NP_001373231.1:p.Val368=
NM_001386303.1:c.1060G=
NP_001373232.1:p.Val354=
NM_001386304.1:c.958G=
NP_001373233.1:p.Val320=
NM_001386305.1:c.922G=
NP_001373234.1:p.Val308=
NM_001386306.1:c.763G=
NP_001373235.1:p.Val255=