Canonical Allele Identifier: CA1881476300
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1016909312
gnomAD v4: 9-130873108-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873108G>C , CM000671.2:g.130873108G>C GRCh38
NC_000009.11:g.133748495G>C , CM000671.1:g.133748495G>C GRCh37
NC_000009.10:g.132738316G>C NCBI36
NG_012034.1:g.164228G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+71G>C ENSP00000361423.2:n.1142+71G>C
ENST00000318560.6:c.1085+71G>C MANE Select ENSP00000323315.5:n.1085+71G>C
ENST00000372348.7:c.1142+71G>C ENSP00000361423.2:n.1142+71G>C
ENST00000318560.5:c.1085+71G>C ENSP00000323315.5:n.1085+71G>C
ENST00000372348.6:c.1142+71G>C ENSP00000361423.2:n.1142+71G>C
NM_005157.5:c.1085+71G>C NP_005148.2:n.1085+71G>C
NM_007313.2:c.1142+71G>C NP_009297.2:n.1142+71G>C
NM_005157.6:c.1085+71G>C MANE Select NP_005148.2:n.1085+71G>C
NM_007313.3:c.1142+71G>C NP_009297.2:n.1142+71G>C
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