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Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.107634463C= , CM000668.2:g.107634463C=
GRCh38
NC_000006.11:g.107955667C= , CM000668.1:g.107955667C=
GRCh37
NC_000006.10:g.108062360C=
NCBI36
NG_028200.1:g.149351C=
NG_028200.2:g.149351C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000317357.10:c.1619C=
MANE Select
ENSP00000318900.5:p.Pro540=
ENST00000317357.9:c.1619C=
ENSP00000318900.5:p.Pro540=
NM_018013.3:c.1619C=
NP_060483.3:p.Pro540=
XM_005267041.3:c.1772C=
XP_005267098.1:p.Pro591=
XM_005267042.3:c.1676C=
XP_005267099.1:p.Pro559=
XM_011535920.1:c.1772C=
XP_011534222.1:p.Pro591=
XM_011535921.1:c.1658C=
XP_011534223.1:p.Pro553=
XM_011535922.1:c.1031C=
XP_011534224.1:p.Pro344=
XM_011535923.1:c.842C=
XP_011534225.1:p.Pro281=
XM_005267041.4:c.1772C=
XP_005267098.1:p.Pro591=
XM_005267042.4:c.1676C=
XP_005267099.1:p.Pro559=
XM_011535920.2:c.1772C=
XP_011534222.1:p.Pro591=
XM_011535921.2:c.1658C=
XP_011534223.1:p.Pro553=
XM_011535923.2:c.842C=
XP_011534225.1:p.Pro281=
XM_017010991.1:c.1172C=
XP_016866480.1:p.Pro391=
XM_017010992.1:c.1172C=
XP_016866481.1:p.Pro391=
XM_017010993.1:c.1172C=
XP_016866482.1:p.Pro391=
XM_017010994.1:c.1172C=
XP_016866483.1:p.Pro391=
NM_018013.4:c.1619C=
MANE Select
NP_060483.3:p.Pro540=