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Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.143728381C>A , CM000670.2:g.143728381C>A
GRCh38
NC_000008.10:g.144810551C>A , CM000670.1:g.144810551C>A
GRCh37
NC_000008.9:g.144882539C>A
NCBI36
NG_016652.1:g.10364G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000388913.4:c.1080G>T
MANE Select
ENSP00000373565.3:p.Pro360=
ENST00000650760.1:c.1683G>T
ENSP00000499217.1:p.Pro561=
ENST00000388913.3:c.1080G>T
ENSP00000373565.3:p.Pro360=
ENST00000395103.2:c.260G>T
NM_198488.3:c.1080G>T
NP_940890.3:p.Pro360=
XM_005250887.2:c.1137G>T
XP_005250944.1:p.Pro379=
XM_005250888.2:c.1098G>T
XP_005250945.1:p.Pro366=
XM_005250889.2:c.1080G>T
XP_005250946.1:p.Pro360=
XM_011516980.1:c.1401G>T
XP_011515282.1:p.Pro467=
XM_011516981.1:c.1248G>T
XP_011515283.1:p.Pro416=
XM_005250887.3:c.1137G>T
XP_005250944.1:p.Pro379=
XM_005250888.3:c.1098G>T
XP_005250945.1:p.Pro366=
XM_005250889.3:c.1080G>T
XP_005250946.1:p.Pro360=
XM_011516980.2:c.1683G>T
XP_011515282.2:p.Pro561=
XM_011516981.2:c.1248G>T
XP_011515283.1:p.Pro416=
XM_024447131.1:c.1080G>T
XP_024302899.1:p.Pro360=
NM_198488.4:c.1080G>T
NP_940890.3:p.Pro360=
NM_198488.5:c.1080G>T
MANE Select
NP_940890.4:p.Pro360=