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Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.104035526C>T , CM000672.2:g.104035526C>T
GRCh38
NC_000010.10:g.105795284C>T , CM000672.1:g.105795284C>T
GRCh37
NC_000010.9:g.105785274C>T
NCBI36
NG_007069.1:g.55355G>A
Transcript Alleles
HGVS
Amino-acid Change
NM_000494.4:c.3456G>A
MANE Select
NP_000485.3:p.Gly1152=
ENST00000648076.2:c.3456G>A
MANE Select
ENSP00000497653.1:p.Gly1152=
NM_000494.3:c.3456G>A
NP_000485.3:p.Gly1152=
ENST00000353479.9:c.3456G>A
ENSP00000340937.5:p.Gly1152=
ENST00000369733.7:c.3321G>A
ENSP00000358748.3:p.Gly1107=
ENST00000369733.8:c.3321G>A
ENSP00000358748.3:p.Gly1107=