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Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.2114539G>A , CM000678.2:g.2114539G>A
GRCh38
NC_000016.9:g.2164540G>A , CM000678.1:g.2164540G>A
GRCh37
NC_000016.8:g.2104541G>A
NCBI36
NG_008617.1:g.26360C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000262304.9:c.2484C>T
MANE Select
ENSP00000262304.4:p.Tyr828=
ENST00000262304.8:c.2484C>T
ENSP00000262304.4:p.Tyr828=
ENST00000423118.5:c.2484C>T
ENSP00000399501.1:p.Tyr828=
ENST00000488185.2:c.472+2950C>T
ENST00000568591.5:c.1415C>T
ENSP00000457162.1:n.1415C>T
NM_000296.3:c.2484C>T
NP_000287.3:p.Tyr828=
NM_001009944.2:c.2484C>T
NP_001009944.2:p.Tyr828=
XM_011522525.1:c.2538C>T
XP_011520827.1:p.Tyr846=
XM_011522526.1:c.2538C>T
XP_011520828.1:p.Tyr846=
XM_011522527.1:c.2538C>T
XP_011520829.1:p.Tyr846=
XM_011522528.1:c.2538C>T
XP_011520830.1:p.Tyr846=
XM_011522529.1:c.2538C>T
XP_011520831.1:p.Tyr846=
XM_011522530.1:c.2484C>T
XP_011520832.1:p.Tyr828=
XM_011522531.1:c.2466C>T
XP_011520833.1:p.Tyr822=
XM_011522532.1:c.2412C>T
XP_011520834.1:p.Tyr804=
XM_011522533.1:c.2331C>T
XP_011520835.1:p.Tyr777=
XM_011522534.1:c.2274C>T
XP_011520836.1:p.Tyr758=
XM_011522535.1:c.360C>T
XP_011520837.1:p.Tyr120=
XM_011522536.1:c.2538C>T
XP_011520838.1:p.Tyr846=
XR_932867.1:n.2553C>T
XR_932868.1:n.2553C>T
XR_932869.1:n.2553C>T
XR_932870.1:n.2553C>T
XM_005255370.3:c.-566C>T
XP_005255427.1:n.-566C>T
XM_011522528.3:c.2538C>T
XP_011520830.1:p.Tyr846=
XM_011522529.2:c.2538C>T
XP_011520831.1:p.Tyr846=
XM_024450298.1:c.2484C>T
XP_024306066.1:p.Tyr828=
XM_024450299.1:c.2412C>T
XP_024306067.1:p.Tyr804=
XM_024450300.1:c.2274C>T
XP_024306068.1:p.Tyr758=
XM_024450301.1:c.360C>T
XP_024306069.1:p.Tyr120=
NM_000296.4:c.2484C>T
NP_000287.4:p.Tyr828=
NM_001009944.3:c.2484C>T
MANE Select
NP_001009944.3:p.Tyr828=