Canonical Allele Identifier: CA361806013
Gene: GM2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.150639453T>A (hg19) chr5:g.151259892T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151259892T>A , CM000667.2:g.151259892T>A GRCh38
NC_000005.9:g.150639453T>A , CM000667.1:g.150639453T>A GRCh37
NC_000005.8:g.150619646T>A NCBI36
NG_009059.1:g.11841T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357164.4:c.219T>A MANE Select ENSP00000349687.3:p.Ser73Arg
ENST00000357164.3:c.219T>A ENSP00000349687.3:p.Ser73Arg
ENST00000523004.1:c.94T>A
ENST00000523466.5:c.264T>A ENSP00000429100.1:p.Ser88Arg
NM_000405.4:c.219T>A NP_000396.2:p.Ser73Arg
NM_001167607.1:c.219T>A NP_001161079.1:p.Ser73Arg
NM_000405.5:c.219T>A MANE Select NP_000396.2:p.Ser73Arg
NM_001167607.2:c.219T>A NP_001161079.1:p.Ser73Arg
NM_001167607.3:c.219T>A NP_001161079.1:p.Ser73Arg
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