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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.72224955G>T , CM000673.2:g.72224955G>T
GRCh38
NC_000011.9:g.71935999G>T , CM000673.1:g.71935999G>T
GRCh37
NC_000011.8:g.71613647G>T
NCBI36
NG_023253.1:g.5118G>T
NG_023253.2:g.5118G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000298229.7:c.-30G>T
MANE Select
ENSP00000298229.2:n.-30G>T
ENST00000298229.6:c.-30G>T
ENSP00000298229.2:n.-30G>T
ENST00000540973.1:c.-30G>T
ENSP00000440904.1:n.-30G>T
ENST00000543234.1:c.-30G>T
ENSP00000440512.1:n.-30G>T
NM_001567.3:c.-30G>T
NP_001558.3:n.-30G>T
XM_005273978.3:c.-30G>T
XP_005274035.1:n.-30G>T
XM_005273979.3:c.-30G>T
XP_005274036.1:n.-30G>T
XM_011544999.1:c.-30G>T
XP_011543301.1:n.-30G>T
XM_011545000.1:c.-30G>T
XP_011543302.1:n.-30G>T
XM_005273979.4:c.-30G>T
XP_005274036.1:n.-30G>T
XM_011544999.2:c.-30G>T
XP_011543301.1:n.-30G>T
XM_024448501.1:c.-30G>T
XP_024304269.1:n.-30G>T
XM_024448502.1:c.-30G>T
XP_024304270.1:n.-30G>T
XM_024448503.1:c.-151G>T
XP_024304271.1:n.-151G>T
XM_024448504.1:c.-30G>T
XP_024304272.1:n.-30G>T
XM_024448505.1:c.-30G>T
XP_024304273.1:n.-30G>T
NM_001567.4:c.-30G>T
MANE Select
NP_001558.3:n.-30G>T