Canonical Allele Identifier: CA350213576
Gene: MARS2 HGNC NCBI

Linked Data

dbSNP Id: rs2089475856
gnomAD v4: 2-197706414-G-C
MyVariant Identifiers: chr2:g.198571138G>C (hg19) chr2:g.197706414G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706414G>C , CM000664.2:g.197706414G>C GRCh38
NC_000002.11:g.198571138G>C , CM000664.1:g.198571138G>C GRCh37
NC_000002.10:g.198279383G>C NCBI36
NG_034122.1:g.6111G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1009G>C MANE Select ENSP00000282276.6:p.Val337Leu
ENST00000282276.7:c.1009G>C ENSP00000282276.6:p.Val337Leu
NM_138395.3:c.1009G>C NP_612404.1:p.Val337Leu
NM_138395.4:c.1009G>C MANE Select NP_612404.1:p.Val337Leu
Search 100 bp 5'
Search 100 bp 3'