Canonical Allele Identifier: CA361807887
Gene: GM2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150646361A>C (hg19) chr5:g.151266800A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151266800A>C , CM000667.2:g.151266800A>C GRCh38
NC_000005.9:g.150646361A>C , CM000667.1:g.150646361A>C GRCh37
NC_000005.8:g.150626554A>C NCBI36
NG_009059.1:g.18749A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357164.4:c.313A>C MANE Select ENSP00000349687.3:p.Ser105Arg
ENST00000357164.3:c.313A>C ENSP00000349687.3:p.Ser105Arg
ENST00000523004.1:c.188A>C
ENST00000523466.5:c.358A>C ENSP00000429100.1:p.Ser120Arg
NM_000405.4:c.313A>C NP_000396.2:p.Ser105Arg
NM_001167607.1:c.313A>C NP_001161079.1:p.Ser105Arg
NM_000405.5:c.313A>C MANE Select NP_000396.2:p.Ser105Arg
NM_001167607.2:c.313A>C NP_001161079.1:p.Ser105Arg
NM_001167607.3:c.313A>C NP_001161079.1:p.Ser105Arg
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