Canonical Allele Identifier: CA515952574
Gene: TASL HGNC NCBI

Linked Data

dbSNP Id: rs887369
MyVariant Identifiers: chrX:g.30577846A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30559729A>G , CM000685.2:g.30559729A>G GRCh38
NC_000023.10:g.30577846A>G , CM000685.1:g.30577846A>G GRCh37
NC_000023.9:g.30487767A>G NCBI36
NG_016375.1:g.23188T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378962.4:c.627T>C MANE Select ENSP00000368245.3:p.Val209=
ENST00000378962.3:c.627T>C ENSP00000368245.3:p.Val209=
NM_025159.2:c.627T>C NP_079435.1:p.Val209=
NM_025159.3:c.627T>C MANE Select NP_079435.1:p.Val209=
Search 100 bp 5'
Search 100 bp 3'