Canonical Allele Identifier: CA5285252
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs556586112
ExAC: 9:133738178 A / G
gnomAD v2: 9-133738178-A-G
gnomAD v3: 9-130862791-A-G
gnomAD v4: 9-130862791-A-G
MyVariant Identifiers: chr9:g.133738178A>G (hg19) chr9:g.130862791A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862791A>G , CM000671.2:g.130862791A>G GRCh38
NC_000009.11:g.133738178A>G , CM000671.1:g.133738178A>G GRCh37
NC_000009.10:g.132727999A>G NCBI36
NG_012034.1:g.153911A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.635A>G ENSP00000361423.2:p.Asn212Ser
ENST00000318560.6:c.578A>G MANE Select ENSP00000323315.5:p.Asn193Ser
ENST00000372348.7:c.635A>G ENSP00000361423.2:p.Asn212Ser
ENST00000318560.5:c.578A>G ENSP00000323315.5:p.Asn193Ser
ENST00000372348.6:c.635A>G ENSP00000361423.2:p.Asn212Ser
NM_005157.5:c.578A>G NP_005148.2:p.Asn193Ser
NM_007313.2:c.635A>G NP_009297.2:p.Asn212Ser
NM_005157.6:c.578A>G MANE Select NP_005148.2:p.Asn193Ser
NM_007313.3:c.635A>G NP_009297.2:p.Asn212Ser
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