Canonical Allele Identifier: CA882866911
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1309009172
gnomAD v4: 19-47004342-C-T
MyVariant Identifiers: chr19:g.47507599C>T (hg19) chr19:g.47004342C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004342C>T , CM000681.2:g.47004342C>T GRCh38
NC_000019.9:g.47507599C>T , CM000681.1:g.47507599C>T GRCh37
NC_000019.8:g.52199439C>T NCBI36
NG_047014.1:g.90776C>T
NG_047014.2:g.148346C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8154C>T ENSP00000385720.2:n.8154C>T
ENST00000672722.1:c.*3654C>T MANE Select ENSP00000500409.1:n.*3654C>T
ENST00000404338.7:c.8154C>T ENSP00000385720.2:n.8154C>T
NM_004491.4:c.8154C>T NP_004482.4:n.8154C>T
NM_004491.5:c.*3654C>T MANE Select NP_004482.4:n.*3654C>T
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