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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173917268A>G , CM000663.2:g.173917268A>G
GRCh38
NC_000001.10:g.173886406A>G , CM000663.1:g.173886406A>G
GRCh37
NC_000001.9:g.172153029A>G
NCBI36
NG_012462.1:g.5111T>C , LRG_577:g.5111T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.-9T>C
MANE Select
ENSP00000356671.3:n.-9T>C
ENST00000367698.3:c.-9T>C
ENSP00000356671.3:n.-9T>C
ENST00000494024.1:n.49T>C
ENST00000617423.4:c.-9T>C
ENSP00000478688.1:n.-9T>C
NM_000488.3:c.-9T>C , LRG_577t1:c.-9T>C
NP_000479.1:n.-9T>C
XM_005245198.2:c.-322T>C
XP_005245255.1:n.-322T>C
NM_001365052.1:c.-322T>C
NP_001351981.1:n.-322T>C
NM_000488.4:c.-9T>C
MANE Select
NP_000479.1:n.-9T>C
NM_001365052.2:c.-322T>C
NP_001351981.1:n.-322T>C
NM_001386302.1:c.-9T>C
NP_001373231.1:n.-9T>C
NM_001386303.1:c.-9T>C
NP_001373232.1:n.-9T>C
NM_001386304.1:c.-9T>C
NP_001373233.1:n.-9T>C
NM_001386305.1:c.-9T>C
NP_001373234.1:n.-9T>C
NM_001386306.1:c.-9T>C
NP_001373235.1:n.-9T>C