Canonical Allele Identifier: CA2959580

Gene: ALB

Linked Data

• dbSNP Id: rs757119484
• ExAC: 4:74280927 A / C
• gnomAD v2: 4-74280927-A-C
• gnomAD v4: 4-73415210-A-C
• MyVariant Identifiers: chr4:g.74280927A>C (hg19) ; chr4:g.73415210A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415210A>C , CM000666.2:g.73415210A>C	GRCh38
NC_000004.11:g.74280927A>C , CM000666.1:g.74280927A>C	GRCh37
NC_000004.10:g.74499791A>C	NCBI36
NG_009291.1:g.15956A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+43A>C MANE Select	ENSP00000295897.4:n.1191+43A>C
ENST00000295897.8:c.1191+43A>C	ENSP00000295897.4:n.1191+43A>C
ENST00000401494.7:c.846+43A>C	ENSP00000384695.3:n.846+43A>C
ENST00000415165.6:c.615+43A>C	ENSP00000401820.2:n.615+43A>C
ENST00000476441.6:c.*470+43A>C	ENSP00000423727.1:n.*470+43A>C
ENST00000484992.1:n.511+43A>C
ENST00000503124.5:c.741+43A>C	ENSP00000421027.1:n.741+43A>C
ENST00000504043.1:n.237A>C
ENST00000505649.5:n.877+43A>C
ENST00000509063.5:c.1191+43A>C	ENSP00000422784.1:n.1191+43A>C
ENST00000511370.1:c.724+43A>C
ENST00000621085.4:c.552+43A>C	ENSP00000483421.1:n.552+43A>C
ENST00000621628.4:c.552+43A>C	ENSP00000480485.1:n.552+43A>C
NM_000477.5:c.1191+43A>C	NP_000468.1:n.1191+43A>C
NM_000477.6:c.1191+43A>C	NP_000468.1:n.1191+43A>C
NM_000477.7:c.1191+43A>C MANE Select	NP_000468.1:n.1191+43A>C