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Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.47995875A>C , CM000674.2:g.47995875A>C
GRCh38
NC_000012.11:g.48389658A>C , CM000674.1:g.48389658A>C
GRCh37
NC_000012.10:g.46675925A>C
NCBI36
NG_008072.1:g.13628T>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000337299.7:c.447T>G
ENSP00000338213.6:p.Pro149=
ENST00000380518.8:c.654T>G
MANE Select
ENSP00000369889.3:p.Pro218=
ENST00000337299.6:c.447T>G
ENSP00000338213.6:p.Pro149=
ENST00000380518.7:c.654T>G
ENSP00000369889.3:p.Pro218=
NM_001844.4:c.654T>G
NP_001835.3:p.Pro218=
NM_033150.2:c.447T>G
NP_149162.2:p.Pro149=
XM_006719242.2:c.798T>G
XP_006719305.2:p.Pro266=
XM_011537928.1:c.798T>G
XP_011536230.1:p.Pro266=
XM_011537929.1:c.798T>G
XP_011536231.1:p.Pro266=
XM_011537930.1:c.798T>G
XP_011536232.1:p.Pro266=
XM_011537931.1:c.798T>G
XP_011536233.1:p.Pro266=
XM_011537932.1:c.798T>G
XP_011536234.1:p.Pro266=
XM_011537933.1:c.798T>G
XP_011536235.1:p.Pro266=
XM_011537934.1:c.795T>G
XP_011536236.1:p.Pro265=
XM_017018828.1:c.798T>G
XP_016874317.1:p.Pro266=
XM_017018829.1:c.795T>G
XP_016874318.1:p.Pro265=
XM_017018830.1:c.588T>G
XP_016874319.1:p.Pro196=
XM_017018831.2:c.108T>G
XP_016874320.1:p.Pro36=
NM_001844.5:c.654T>G
MANE Select
NP_001835.3:p.Pro218=
NM_033150.3:c.447T>G
NP_149162.2:p.Pro149=