Canonical Allele Identifier: CA2586004317
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004394-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004394G>T , CM000681.2:g.47004394G>T GRCh38
NC_000019.9:g.47507651G>T , CM000681.1:g.47507651G>T GRCh37
NC_000019.8:g.52199491G>T NCBI36
NG_047014.1:g.90828G>T
NG_047014.2:g.148398G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8206G>T ENSP00000385720.2:n.8206G>T
ENST00000672722.1:c.*3706G>T MANE Select ENSP00000500409.1:n.*3706G>T
ENST00000404338.7:c.8206G>T ENSP00000385720.2:n.8206G>T
NM_004491.4:c.8206G>T NP_004482.4:n.8206G>T
NM_004491.5:c.*3706G>T MANE Select NP_004482.4:n.*3706G>T
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