Canonical Allele Identifier: CA170814
Gene: ALB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73417671T>C , CM000666.2:g.73417671T>C GRCh38
NC_000004.11:g.74283388T>C , CM000666.1:g.74283388T>C GRCh37
NC_000004.10:g.74502252T>C NCBI36
NG_009291.1:g.18417T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1428+2T>C MANE Select ENSP00000295897.4:n.1428+2T>C
ENST00000295897.8:c.1428+2T>C ENSP00000295897.4:n.1428+2T>C
ENST00000401494.7:c.1083+2T>C ENSP00000384695.3:n.1083+2T>C
ENST00000415165.6:c.852+2T>C ENSP00000401820.2:n.852+2T>C
ENST00000476441.6:c.*707+2T>C ENSP00000423727.1:n.*707+2T>C
ENST00000503124.5:c.978+2T>C ENSP00000421027.1:n.978+2T>C
ENST00000505649.5:n.976-417T>C
ENST00000509063.5:c.1428+2T>C ENSP00000422784.1:n.1428+2T>C
ENST00000511370.1:c.961+2T>C
ENST00000621085.4:c.789+2T>C ENSP00000483421.1:n.789+2T>C
ENST00000621628.4:c.789+2T>C ENSP00000480485.1:n.789+2T>C
NM_000477.5:c.1428+2T>C NP_000468.1:n.1428+2T>C
NM_000477.6:c.1428+2T>C NP_000468.1:n.1428+2T>C
NM_000477.7:c.1428+2T>C MANE Select NP_000468.1:n.1428+2T>C
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