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Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.18130781C= , CM000668.2:g.18130781C=
GRCh38
NC_000006.11:g.18131012C= , CM000668.1:g.18131012C=
GRCh37
NC_000006.10:g.18238991C=
NCBI36
NG_012137.2:g.29363G=
NG_012137.3:g.29363G=
Transcript Alleles
HGVS
Amino-acid Change
NM_000367.5:c.626-1G=
MANE Select
NP_000358.1:n.626-1G=
ENST00000309983.5:c.626-1G=
MANE Select
ENSP00000312304.4:n.626-1G=
NM_000367.3:c.626-1G=
NP_000358.1:n.626-1G=
NM_000367.4:c.626-1G=
NP_000358.1:n.626-1G=
NM_001346817.1:c.626-1G=
NP_001333746.1:n.626-1G=
NM_001346818.1:c.581-1G=
NP_001333747.1:n.581-1G=
ENST00000309983.4:c.626-1G=
ENSP00000312304.4:n.626-1G=
XM_011514839.1:c.581-1G=
XP_011513141.1:n.581-1G=
XM_011514840.1:c.557-1G=
XP_011513142.1:n.557-1G=