Canonical Allele Identifier: CA1931513247
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845309A= , CM000672.2:g.99845309A= GRCh38
NC_000010.10:g.101605066A= , CM000672.1:g.101605066A= GRCh37
NC_000010.9:g.101595056A= NCBI36
NG_011798.1:g.67604A=
NG_011798.2:g.67712A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3988-315A= MANE Select ENSP00000497274.1:n.3988-315A=
ENST00000649459.1:n.336-315A=
ENST00000370449.8:c.3988-315A= ENSP00000359478.4:n.3988-315A=
NM_000392.4:c.3988-315A= NP_000383.1:n.3988-315A=
XM_006717630.2:c.3292-315A= XP_006717693.1:n.3292-315A=
XR_945604.1:n.4177-374A=
XR_945605.1:n.4052-315A=
NM_000392.5:c.3988-315A= MANE Select NP_000383.2:n.3988-315A=
XM_006717630.3:c.3292-315A= XP_006717693.1:n.3292-315A=
XR_945604.3:n.4231-374A=
XR_945605.3:n.4104-315A=
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