Canonical Allele Identifier: CA447180334
Gene: GM2A HGNC NCBI

Linked Data

gnomAD v4: 5-151266811-T-C
MyVariant Identifiers: chr5:g.150646372T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151266811T>C , CM000667.2:g.151266811T>C GRCh38
NC_000005.9:g.150646372T>C , CM000667.1:g.150646372T>C GRCh37
NC_000005.8:g.150626565T>C NCBI36
NG_009059.1:g.18760T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357164.4:c.324T>C MANE Select ENSP00000349687.3:p.Phe108=
ENST00000357164.3:c.324T>C ENSP00000349687.3:p.Phe108=
ENST00000523004.1:c.199T>C
ENST00000523466.5:c.369T>C ENSP00000429100.1:p.Phe123=
NM_000405.4:c.324T>C NP_000396.2:p.Phe108=
NM_001167607.1:c.324T>C NP_001161079.1:p.Phe108=
NM_000405.5:c.324T>C MANE Select NP_000396.2:p.Phe108=
NM_001167607.2:c.324T>C NP_001161079.1:p.Phe108=
NM_001167607.3:c.324T>C NP_001161079.1:p.Phe108=
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