Canonical Allele Identifier: CA10990384
Gene: RASAL2 HGNC NCBI

Linked Data

dbSNP Id: rs316274
gnomAD v2: 1-178142208-G-A
gnomAD v3: 1-178173073-G-A
gnomAD v4: 1-178173073-G-A
MyVariant Identifiers: chr1:g.178142208G>A (hg19) chr1:g.178173073G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.178173073G>A , CM000663.2:g.178173073G>A GRCh38
NC_000001.10:g.178142208G>A , CM000663.1:g.178142208G>A GRCh37
NC_000001.9:g.176408831G>A NCBI36
NG_047109.1:g.84345G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367649.8:c.202+78379G>A MANE Select ENSP00000356621.3:n.202+78379G>A
ENST00000367649.7:c.202+78379G>A ENSP00000356621.3:n.202+78379G>A
ENST00000465723.1:n.526+47572G>A
NM_170692.2:c.202+78379G>A NP_733793.2:n.202+78379G>A
XM_011510166.1:c.202+78379G>A XP_011508468.1:n.202+78379G>A
XM_011510167.1:c.202+78379G>A XP_011508469.1:n.202+78379G>A
XM_011510168.1:c.202+78379G>A XP_011508470.1:n.202+78379G>A
XM_011510166.2:c.202+78379G>A XP_011508468.1:n.202+78379G>A
XM_011510167.2:c.202+78379G>A XP_011508469.1:n.202+78379G>A
NM_170692.4:c.202+78379G>A MANE Select NP_733793.2:n.202+78379G>A
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