Canonical Allele Identifier: CA260660767
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs955339719
MyVariant Identifiers: chr14:g.50088708T>C (hg19) chr14:g.49621990T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621990T>C , CM000676.2:g.49621990T>C GRCh38
NC_000014.8:g.50088708T>C , CM000676.1:g.50088708T>C GRCh37
NC_000014.7:g.49158458T>C NCBI36
NG_008920.1:g.6220T>C
NG_033054.1:g.3642A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.722T>C MANE Select ENSP00000307423.2:p.Val241Ala
ENST00000305386.3:c.722T>C ENSP00000307423.2:p.Val241Ala
NM_002408.3:c.722T>C NP_002399.1:p.Val241Ala
NM_002408.4:c.722T>C MANE Select NP_002399.1:p.Val241Ala
Search 100 bp 5'
Search 100 bp 3'