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Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.8122015G>T , CM000679.2:g.8122015G>T
GRCh38
NC_000017.10:g.8025333G>T , CM000679.1:g.8025333G>T
GRCh37
NC_000017.9:g.7966058G>T
NCBI36
NG_015807.1:g.1902C>A
NG_015816.1:g.7078C>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000541682.7:c.249C>A
MANE Select
ENSP00000446205.2:p.Pro83=
ENST00000317814.8:c.234C>A
ENSP00000314774.4:p.Pro78=
ENST00000541682.6:c.249C>A
ENSP00000446205.2:p.Pro83=
ENST00000577735.1:c.225C>A
ENSP00000462491.1:p.Pro75=
NM_001165967.1:c.249C>A
NP_001159439.1:p.Pro83=
NM_032580.3:c.234C>A
NP_115969.2:p.Pro78=
XM_011524038.1:c.354C>A
XP_011522340.1:p.Pro118=
XM_011524039.1:c.345C>A
XP_011522341.1:p.Pro115=
XM_011524040.1:c.345C>A
XP_011522342.1:p.Pro115=
XM_011524041.1:c.336C>A
XP_011522343.1:p.Pro112=
XM_011524042.1:c.207C>A
XP_011522344.1:p.Pro69=
XR_934203.1:n.69+2201G>T
XM_017025232.1:c.354C>A
XP_016880721.1:p.Pro118=
XM_024451007.1:c.354C>A
XP_024306775.1:p.Pro118=
NM_001165967.2:c.249C>A
MANE Select
NP_001159439.1:p.Pro83=
NM_032580.4:c.234C>A
NP_115969.2:p.Pro78=