Canonical Allele Identifier: CA309123881
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs868438639
MyVariant Identifiers: chr19:g.47507094T>G (hg19) chr19:g.47003837T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003837T>G , CM000681.2:g.47003837T>G GRCh38
NC_000019.9:g.47507094T>G , CM000681.1:g.47507094T>G GRCh37
NC_000019.8:g.52198934T>G NCBI36
NG_047014.1:g.90271T>G
NG_047014.2:g.147841T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7649T>G ENSP00000385720.2:n.7649T>G
ENST00000672722.1:c.*3149T>G MANE Select ENSP00000500409.1:n.*3149T>G
ENST00000404338.7:c.7649T>G ENSP00000385720.2:n.7649T>G
ENST00000614079.1:c.7226T>G ENSP00000483730.1:n.7226T>G
NM_004491.4:c.7649T>G NP_004482.4:n.7649T>G
NM_004491.5:c.*3149T>G MANE Select NP_004482.4:n.*3149T>G
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